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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 80 of 104

Device	Model / Reference	Registries	Class	Status
Endo Carry-on Procedure Kit	4009905	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009802	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4008952	FDA UDI	Class II	Active
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Endo-Carry-on Procedure Kit	4006511	FDA UDI	Class II	Active
Custom Procedure Kit	4000383	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-107425-0002	FDA UDI	Class I	Unknown
Custom Procedure Kit	4000582	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-109629-0001	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-104531-0002	FDA UDI	Class I	Unknown
Trial Procedure Kit	CPKT-894200-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-100727-0009	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-102119-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-101961-0003	FDA UDI	Class I	Unknown
Preclean Kit	4000890	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	101823	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-137550-0002	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-200290-0002	FDA UDI	Class II	Active
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Custom Procedure Kit	4004017	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4007935	FDA UDI	Class II	Active
Custom Procedure Kit	CPK-200651-0001	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-103398-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-106815-0001	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-238500-0002	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009696	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008337	FDA UDI	Class II	Active
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Custom Procedure Kit	4000668	FDA UDI	Class I	Unknown
Custom Procedure Kit	4000960	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4007568	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009372	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009729	FDA UDI	Class II	Active
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Endo-Carry-on Procedure Kit	4008363	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009899	FDA UDI	Class II	Active
Custom Procedure Kit	4003568	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-820600-0001	FDA UDI	Class I	Unknown
Custom Procedure Kit	4000842	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-103015-0004	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-104232-0004	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-238500-0003	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Custom Procedure Kit	CPK-106590-0002	FDA UDI	Class I	Unknown
Custom Procedure Kit	4001093	FDA UDI	Class I	Unknown
Trial Procedure Kit	CPKT-110359-0001	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4010185	FDA UDI	Class II	Active
Custom Procedure Kit	4002489	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.