Is this your brand? Sign in to claim ownership.

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 52 of 104

Device	Model / Reference	Registries	Class	Status
Trial Procedure Kit	CPKT-102659-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	101804	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008348	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	100998	FDA UDI	Class I	Unknown
Custom Procedure Kit	4000790	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-205390-0006	FDA UDI	Class I	Unknown
Centrisol Acid Concentrate	SB-127	FDA UDI	Class II	Unknown
Custom Procedure Kit	4004870	FDA UDI	Class II	Active
Custom Procedure Kit	4000651	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4008857	FDA UDI	Class II	Active
Custom Procedure Kit	4003932	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-200793-0001	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
EcoNotrap 2 Double Chamber Polyp Trap	100102	FDA UDI	Class II	Unknown
Endo-Carry-on Procedure Kit	4006157	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008146	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4008975	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-844500-0003	FDA UDI	Class I	Unknown
Custom Procedure Kit	4002921	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009005	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009219	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPKT-103773-0012	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4007703	FDA UDI	Class II	Active
Custom Procedure Kit	4002530	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009100	FDA UDI	Class II	Active
Custom Procedure Kit	4003953	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4010381	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-108999-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-108839-0001	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Trial Procedure Kit	CPKT-100100-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	101924	FDA UDI	Class I	Unknown
Cleanascope/Defendo-Bund	580305	FDA UDI	Class I	Active
Endo Carry-On Procedure Kit	CPK-111075-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-101215-0011	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-499900-0002	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4008047	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009864	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4006845	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008305	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-104104-0001	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009933	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009979	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4010055	FDA UDI	Class II	Active
Custom Procedure Kit	4002638	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009847	FDA UDI	Class II	Active
Preclean Kit	4001123	FDA UDI	Class II	Active
Custom Procedure Kit	CPK-101018-0001	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Medivators Hookup	Hookup	FDA UDI	Class II	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.