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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 95 of 104

Device	Model / Reference	Registries	Class	Status
Endo Carry-On Procedure Kit	100858	FDA UDI	Class I	Unknown
Custom Procedure Kit	CPK-844500-0007	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4006181	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008210	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009896	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-603520-0001	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008219	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-599500-0002	FDA UDI	Class I	Unknown
Custom Procedure Kit	4000124	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-106585-0002	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-110450-0003	FDA UDI	Class I	Unknown
Custom Procedure Kit	4002870	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-103015-0003	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-105167-0001	FDA UDI	Class II	Active
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Endo-Carry-on Procedure Kit	4008197	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009857	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-105802-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-106258-0002	FDA UDI	Class II	Active
Custom Procedure Kit	4000744	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4007723	FDA UDI	Class II	Active
Custom Procedure Kit	4004346	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-822905-0002	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4007355	FDA UDI	Class II	Active
Custom Procedure Kit	4000055	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4007361	FDA UDI	Class II	Active
Custom Procedure Kit	4001428	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-111224-0002	FDA UDI	Class I	Unknown
Custom Procedure Kit	4000630	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-110492-0002	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-100797-0005	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009769	FDA UDI	Class II	Active
Custom Procedure Kit	4000221	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4010535	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-820660-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	101890	FDA UDI	Class II	Active
FiberFlo	93022-016	FDA UDI	Class II	Unknown
Trial Procedure Kit	CPKT-101048-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-108672-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-103773-0020	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009725	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4006131	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008214	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009852	FDA UDI	Class II	Active
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Essential Kit	4000912	FDA UDI	Class II	Active
Custom Procedure Kit	4000426	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009183	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-104854-0011	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.