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Centurion Medical Products

Last updated May 23, 2026

What Centurion Medical Products makes

Centurion Medical Products manufactures single-use surgical procedure kits, including general surgical kits (both medicated and non-medicated), central venous catheterization kits, circumcision kits, peripheral intravenous catheterization support kits, ENT surgical kits, birthing/delivery kits, and procedural medication labeling sets.

The company's portfolio consists of Class I and Class II medical devices, which are listed in the FDA Unique Device Identifier (UDI) registry. Centurion Medical Products is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What medical devices does Centurion Medical Products manufacture?

Centurion Medical Products manufactures single-use surgical procedure kits including general surgical kits (medicated and non-medicated), central venous catheterization kits, circumcision kits, peripheral intravenous catheterization support kits, ENT surgical kits, birthing/delivery kits, and procedural medication labeling sets.

Where is Centurion Medical Products based?

Centurion Medical Products is based in the United States, as indicated in the device registry information.

Which regulatory registries list Centurion Medical Products' devices?

Centurion Medical Products' devices are listed in the FDA Unique Device Identifier (UDI) registry, which tracks medical devices marketed in the United States.

How are Centurion Medical Products' devices classified?

Centurion Medical Products manufactures Class I and Class II medical devices, with Class I being lower risk and Class II requiring more regulatory controls than Class I devices.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: US
Address: —
Website: —
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Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: —

Catalogue (11015)

Page 4 of 221

Device	Model / Reference	Registries	Class	Status
Centurion	IG18TST	FDA UDI	Class I	Active
Centurion	PE125	FDA UDI	Class II	Active
Centurion	SUT885	FDA UDI	Class I	Active
Centurion	MNS3870	FDA UDI	Class I	Active
Medline Industries, Inc.	CMP-M85164L-B	FDA UDI	Class II	Active
Centurion	SUT18770	FDA UDI	Class I	Active
Centurion	ECVC3275	FDA UDI	Class II	Active
Centurion	ID615	FDA UDI	Class I	Active
Medline Industries, Inc.	ECVC930	FDA UDI	Class II	Active
Medline Industries, Inc.	ECVC1845	FDA UDI	Class II	Active
Centurion	CIT2510	FDA UDI	Class II	Active
Medline	RWM-DC573KC	FDA UDI	Class I	Active
Centurion	ART210	FDA UDI	Class II	Active
Centurion	CHT1780	FDA UDI	Class I	Active
Centurion	MNS11360	FDA UDI	Class I	Active
Centurion	CHT1385	FDA UDI	Class I	Active
Centurion	CIT4235	FDA UDI	Class II	Active
Centurion	SPSY007	FDA UDI	Class II	Active
Centurion	SUT12025	FDA UDI	Class I	Active
Centurion	DM470A	FDA UDI	Class I	Active
Centurion	TC7995	FDA UDI	Class I	Active
Centurion	ID1875	FDA UDI	Class I	Active
Centurion	STL2688	FDA UDI	Class I	Active
Centurion	BSK105	FDA UDI	Class I	Active
Centurion	DT10925	FDA UDI	Class I	Active
Centurion	BP180	FDA UDI	Class I	Active
Centurion	SR245	FDA UDI	Class I	Active
Centurion	IVS4160	FDA UDI	Class II	Active
Centurion	STCVC2005	FDA UDI	Class II	Active
Centurion	MNS10835	FDA UDI	Class I	Active
Medline	DYKM1751	FDA UDI	Class I	Active
Centurion	CIT6755A	FDA UDI	Class II	Active
Medline Industries, Inc.	ECVC6075	FDA UDI	Class II	Active
Centurion	I86530	FDA UDI	Class I	Active
Centurion	STL1811	FDA UDI	Class I	Active
Centurion	SUT20535	FDA UDI	Class I	Active
Medline Industries, Inc.	I550BF7C	FDA UDI	Class II	Active
Centurion	ECVC7050	FDA UDI	Class II	Active
Centurion	HGL4	FDA UDI	Class I	Active
Centurion	STL2163	FDA UDI	Class I	Active
Centurion	TC8015	FDA UDI	Class I	Active
Centurion	DT18750A	FDA UDI	Class I	Active
Centurion	PE2565A	FDA UDI	Class II	Active
Centurion	75705	FDA UDI	Class I	Active
Centurion	STL2022	FDA UDI	Class I	Active
Centurion	EART60ST	FDA UDI	Class I	Active
Centurion	STL1107	FDA UDI	Class I	Active
Centurion	UVT280	FDA UDI	Class I	Active
Centurion	ID1905	FDA UDI	Class I	Active
Centurion	PE2635A	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (100)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Centurion Medical Products has 286 recall records initiated between September 22, 2009, and December 11, 2019, all with a status of terminated. The reasons for recall include issues such as compromised sterile packaging, potential for package integrity problems, recalls of components from suppliers due to various concerns like particulate matter, incomplete documentation, and contamination risks. Some recalls were initiated as sub-recalls for products contained in kits that were being recalled by their original manufacturers.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Dec 11, 2019	Z-1075-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1059-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1042-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1082-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1063-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1087-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1068-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1081-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1064-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1083-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1049-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1058-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1047-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1084-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1091-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1053-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1079-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1089-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1052-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1095-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1055-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1050-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1045-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1070-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1094-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1066-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1061-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1065-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1086-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1062-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1051-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1085-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1057-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1060-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1067-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1073-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1044-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1092-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1054-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1056-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1077-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1043-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1088-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1080-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1074-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1076-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1078-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1071-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1069-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1048-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1072-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1090-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1046-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Dec 11, 2019	Z-1093-2020	—	terminated	Incomplete seals on the sterile package may compromise the sterility
Oct 24, 2019	Z-0344-2020	—	terminated	Sterile packaging incomplete seals may compromise sterility of the product
Aug 28, 2019	Z-0120-2020	—	terminated	A mismatch between the angle of the hole in the base and the angle of the bell, which may cause the clamp to remove foreskin without the use of a scalpel.
Aug 28, 2019	Z-0121-2020	—	terminated	A mismatch between the angle of the hole in the base and the angle of the bell, which may cause the clamp to remove foreskin without the use of a scalpel.
Jul 15, 2019	Z-0254-2020	—	terminated	Supplier initiated recall of the GRIPPER Needles
Jul 15, 2019	Z-0255-2020	—	terminated	Supplier initiated recall of the GRIPPER Needles
Jul 15, 2019	Z-0256-2020	—	terminated	Supplier initiated recall of the GRIPPER Needles
Jul 15, 2019	Z-0253-2020	—	terminated	Supplier initiated recall of the GRIPPER Needles
Jul 1, 2019	Z-2165-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2166-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2164-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2171-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2161-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2170-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2168-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2167-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2162-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2172-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2163-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2173-2019	—	terminated	Potential for sterile packaging to be compromised
Jul 1, 2019	Z-2169-2019	—	terminated	Potential for sterile packaging to be compromised
Jun 24, 2019	Z-0407-2020	—	terminated	Various medical device kits contain MAJOR Nasal Decongestant Spray is being recalled by the manufacturer
Jun 24, 2019	Z-0408-2020	—	terminated	Various medical device kits contain MAJOR Nasal Decongestant Spray is being recalled by the manufacturer.
Jun 24, 2019	Z-0409-2020	—	terminated	Various medical device kits contain MAJOR Nasal Decongestant Spray is being recalled by the manufacturer.
Jun 7, 2019	Z-1956-2019	—	terminated	Centurion is conducting a sub-recall for Teleflex Sheridan branded Endotracheal Tracheal Tubes due to increased incidence of Sheridan connector becoming disconnected from Endotracheal Tube.
Jun 1, 2019	Z-2545-2020	—	terminated	False elevation of carboxyhemoglobin (COHb) results in blood samples collected using BD Vacutainer Plastic Lithium Heparin tubes with the IL GEM 4000 instrument.
Apr 24, 2019	Z-0080-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0102-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0103-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0084-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0094-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0081-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0086-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0077-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0085-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0090-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0083-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0075-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0092-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0087-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0105-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0098-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0093-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0106-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0078-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0076-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Apr 24, 2019	Z-0096-2020	—	terminated	Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.