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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 45 of 104

Device	Model / Reference	Registries	Class	Status
Endo-Carry-on Procedure Kit	4006142	FDA UDI	Class II	Active
Custom Procedure Kit	4000223	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-108327-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-136300-0003	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-200169-0002	FDA UDI	Class I	Unknown
Trial Procedure Kit	CPKT-106480-0001	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009766	FDA UDI	Class II	Active
Custom Procedure Kit	4003050	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-107334-0004	FDA UDI	Class I	Unknown
Custom Procedure Kit	4000087	FDA UDI	Class II	Active
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Trial Procedure Kit	CPKT-101864-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-103773-0009	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4010610	FDA UDI	Class II	Active
Custom Procedure Kit	CPK-111456-0004	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009894	FDA UDI	Class II	Active
Custom Procedure Kit	4000857	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009164	FDA UDI	Class II	Active
Preclean Kit	4000902	FDA UDI	Class II	Active
Custom Procedure Kit	CPK-107324-0010	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4008365	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4007280	FDA UDI	Class II	Active
Custom Procedure Kit	4001527	FDA UDI	Class II	Active
Preclean Kit	4000895	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-102730-0002	FDA UDI	Class I	Unknown
Endo Carry-On Transport Pad	101800	FDA UDI	Class I	Active
Endo Carry-On Procedure Kit	CPK-104282-0001	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Custom Procedure Kit	4005627	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4006536	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009449	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4005927	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-103966-0003	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-200665-0001	FDA UDI	Class II	Active
Custom Procedure Kit	4000190	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	100873	FDA UDI	Class I	Unknown
Custom Procedure Kit	4003871	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4008962	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-100061-0001	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-106846-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-101241-0002	FDA UDI	Class I	Unknown
Trial Procedure Kit	CPKT-571714-0001	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	101976	FDA UDI	Class I	Unknown
FiberFlo	93022-028	FDA UDI	Class II	Unknown
Endo Carry-On Procedure Kit	CPKT-339347-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-667000-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-914700-0005	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	101832	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4008739	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.