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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 74 of 104

Device	Model / Reference	Registries	Class	Status
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4010455	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008421	FDA UDI	Class II	Active
Custom Procedure Kit	4000271	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4006538	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-606051-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-298000-0002	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-106672-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-100680-0003	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	101969	FDA UDI	Class II	Active
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
ENDOGATOR Kit	100653B	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-200169-0003	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-470015-0001	FDA UDI	Class I	Unknown
Custom Procedure Kit	4004372	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009346	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-457000-0004	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-100815-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-107842-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-104106-0001	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009520	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-105107-0001	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	4001290	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4010551	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-881020-0002	FDA UDI	Class I	Unknown
Essential Kit	4001130	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4007123	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009697	FDA UDI	Class II	Active
Essential Kit	4000935	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-106389-0001	FDA UDI	Class I	Unknown
FiberFlo	93023-144	FDA UDI	Class II	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Trial Procedure Kit	CPKT-104232-0002	FDA UDI	Class I	Unknown
Custom Procedure Kit	4002688	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4007144	FDA UDI	Class II	Active
Centrisol Acid Concentrate	SB-352	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008133	FDA UDI	Class II	Active
Endo Carry-on Custom Procedure Kit	4005775	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-103423-0001	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPKT-912220-0003	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	100832	FDA UDI	Class I	Unknown
Double Ended Channel Brush	100402	FDA UDI	Class I	Active
Endo Carry-on Procedure Kit	4009817	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009169	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008043	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009358	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.