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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 32 of 104

Device	Model / Reference	Registries	Class	Status
Endo Carry-On Procedure Kit	102864	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-660000-0002	FDA UDI	Class I	Unknown
Trial Procedure Kit	CPKT-110207-0004	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Custom Procedure Kit	4000239	FDA UDI	Class II	Active
EndoGator Hybrid	4003168	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4006285	FDA UDI	Class II	Active
Custom Procedure Kit	4001285	FDA UDI	Class II	Active
ENDOGATOR hybrid irrigation tubing	100606	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-106778-0001	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-102138-0003-33	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4007789	FDA UDI	Class II	Active
Custom Procedure Kit	4003561	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-103407-0002	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009349	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	101904	FDA UDI	Class I	Unknown
Custom Procedure Kit	CPK-104330-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-200487-0001	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-457000-0005	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-108226-0004-33	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	101917	FDA UDI	Class II	Active
ENDOGATOR Kit	100622	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008114	FDA UDI	Class II	Active
Custom Procedure Kit	4000132	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-105123-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-105070-0004	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009373	FDA UDI	Class II	Active
Endo Carry-On Transport Pad	100800	FDA UDI	Class I	Active
Endo-Carry-on Procedure Kit	4008130	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4007733	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-102655-0001	FDA UDI	Class II	Active
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Centrisol Acid Concentrate	SB-142	FDA UDI	Class II	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Custom Procedure Kit	4010526	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-251200-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	100917	FDA UDI	Class II	Active
Endogator	100115B	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	101920	FDA UDI	Class I	Unknown
Custom Procedure Kit	4000060	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009414	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-110585-0003	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-104648-0003	FDA UDI	Class II	Active
FiberFlo	93250-127	FDA UDI	Class II	Unknown
Endo Carry-On Procedure Kit	CPKT-100797-0001	FDA UDI	Class I	Unknown
Waterjet Connector	100242P	FDA UDI	Class II	Unknown
Endo Carry-on Procedure Kit	4009112	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009941	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008835	FDA UDI	Class II	Active
Custom Procedure Kit	4002623	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.