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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 81 of 104

Device	Model / Reference	Registries	Class	Status
Endo Carry-on Procedure Kit	4010281	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-697040-0001	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-200044-0001	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008563	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4010559	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-107330-0007	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4010026	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-104266-0001	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-102669-0002	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4008963	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-107437-0002-33	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009067	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPKT-100797-0002	FDA UDI	Class I	Unknown
Minncare HD	3031105	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-106370-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-339347-0001-33	FDA UDI	Class I	Unknown
ENDOGATOR hybrid irrigation tubing	100609	FDA UDI	Class II	Active
ENDOGATOR Kit	100623	FDA UDI	Class II	Active
Custom Procedure Kit	4001322	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	101915	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-100330-0002	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-102559-0001	FDA UDI	Class I	Unknown
FiberFlo	93022-141	FDA UDI	Class II	Unknown
Endo Carry-On Procedure Kit	CPK-103857-0003	FDA UDI	Class I	Unknown
Trial Procedure Kit	CPKT-200427-0003	FDA UDI	Class I	Unknown
EndoGator Hybrid	4003176	FDA UDI	Class II	Active
Custom Procedure Kit	CPK-583400-0001	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Endo Carry-on Procedure Kit	4009695	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4006155	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-104323-0001	FDA UDI	Class I	Unknown
Trial Procedure Kit	CPKT-100717-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-104854-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	102824	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-105641-0001	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4010596	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-914700-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-111479-0001	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-200169-0004	FDA UDI	Class I	Unknown
Custom Procedure Kit	4002339	FDA UDI	Class II	Active
Custom Procedure Kit	CPK-457000-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-106196-0001	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Custom Procedure Kit	4000261	FDA UDI	Class II	Active
Centrisol Acid Concentrate	SB-164	FDA UDI	Class II	Active
Custom Procedure Kit	4003087	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-105928-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-829600-0001	FDA UDI	Class I	Unknown
Trial Procedure Kit	CPKT-104614-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	101886	FDA UDI	Class I	Unknown

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.