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MEDIVATORS INC.

United States·US-MF-000043422

Last updated September 17, 2026

Information

Country: United States
Address: 3150, Pollok Dr, Conroe, United States
Website: www.steris.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1(800)444-4729
PRRC Contact: Zeeshan Shamim
EUDAMED SRN: US-MF-000043422
FDA FEI Number: 3003012447
DUNS Number: 068199363

Catalogue (5153)

Page 24 of 104

Device	Model / Reference	Registries	Class	Status
Endo Carry-On Procedure Kit	102836	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-105330-0001	FDA UDI	Class I	Unknown
Endogator	200230F	FDA UDI	Class II	Unknown
Endo Carry-on Procedure Kit	4010540	FDA UDI	Class II	Active
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009160	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-108075-0001	FDA UDI	Class I	Unknown
DEFENDO Disposable Biopsy Valve	100319	FDA UDI	Class II	Unknown
Endo Carry-on Procedure Kit	4009891	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-107760-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-949400-0003	FDA UDI	Class I	Unknown
Centrisol Acid Concentrate	SB-111	FDA UDI	Class II	Unknown
Trial Procedure Kit	CPKT-108984-0004	FDA UDI	Class I	Unknown
Trial Procedure Kit	CPKT-107196-0001	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-949400-0002	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009196	FDA UDI	Class II	Active
Intercept Foam	ML020139	FDA UDI	Class I	Active
Endo Carry-on Procedure Kit	4010677	FDA UDI	Class II	Active
Custom Procedure Kit	CPK-103941-0001	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009993	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008239	FDA UDI	Class II	Active
Custom Procedure Kit	4003350	FDA UDI	Class II	Active
Endo Smartcap	4005098	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-105192-0002	FDA UDI	Class I	Unknown
Trial Procedure Kit	CPKT-105638-0001	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4007491	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-736500-0008	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-455700-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-104191-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-251200-0004	FDA UDI	Class I	Unknown
Custom Procedure Kit	4003896	FDA UDI	Class II	Active
Custom Procedure Kit	4001499	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-103352-0007	FDA UDI	Class I	Unknown
Trial Procedure Kit	CPKT-104604-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-200843-0004	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4009022	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009914	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-200106-0001	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4010228	FDA UDI	Class II	Active
Custom Procedure Kit	CPK-918616-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-491013-0003	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	200804A	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-107324-0001	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4010631	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-101961-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-106408-0007	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008602	FDA UDI	Class II	Active
Custom Procedure Kit	4003230	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

STERIS Ireland Ltd IE

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (9)

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

Date	Recall No.	Class	Status	Reason
Apr 20, 2021	Z-1859-2021	—	terminated	The lot may have experienced an anomaly during the manufacturing process, that could lead to an out of specification concentrate formulation.
Oct 9, 2019	Z-1775-2020	—	terminated	Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.
Oct 9, 2019	Z-1777-2020	—	terminated	Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.
Oct 9, 2019	Z-1774-2020	—	terminated	Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.
Oct 9, 2019	Z-1773-2020	—	terminated	Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.
Oct 9, 2019	Z-1776-2020	—	terminated	Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.
Oct 9, 2019	Z-1772-2020	—	terminated	Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.
Oct 9, 2019	Z-1778-2020	—	terminated	Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.
Aug 3, 2015	Z-2761-2015	—	terminated	Hemoconcentrators may exhibit low ultrafiltration performance that is below product specification.