Is this your brand? Sign in to claim ownership.

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 44 of 104

Device	Model / Reference	Registries	Class	Status
Endo Carry-On Procedure Kit	CPK-500175-0003	FDA UDI	Class I	Unknown
Essential Kit	4000918	FDA UDI	Class II	Active
Custom Procedure Kit	4000858	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-583050-0003	FDA UDI	Class I	Unknown
Endo Carry-on Custom Procedure Kit	4005905	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-200654-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-200802-0002	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	101949	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-105164-0003	FDA UDI	Class II	Active
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Custom Procedure Kit	CPK-108713-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-104623-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-104854-0008	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-104019-0002-33	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Endo-Carry-on Procedure Kit	4008004	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4010404	FDA UDI	Class II	Active
FiberFlo	93250-070	FDA UDI	Class II	Unknown
Custom Procedure Kit	CPK-110675-0002	FDA UDI	Class I	Unknown
Custom Procedure Kit	4002626	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009983	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009195	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4007853	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-369030-0004	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-647350-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-200201-0001	FDA UDI	Class II	Active
Custom Procedure Kit	4003403	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4010181	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-105694-0001	FDA UDI	Class I	Unknown
Trial Procedure Kit	CPKT-107402-0001	FDA UDI	Class I	Unknown
Preclean Kit	4000891	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-200682-0001-33	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4007979	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-100330-0001	FDA UDI	Class I	Unknown
Trial Procedure Kit	CPKT-109987-0001	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
FiberFlo	93023-139	FDA UDI	Class II	Unknown
Endo Carry-on Procedure Kit	4010430	FDA UDI	Class II	Active
Custom Procedure Kit	CPK-103773-0025	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	101909	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPKT-103773-0010	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-102044-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-104091-0001	FDA UDI	Class I	Unknown
Dsd-201	DSD-201 120V	FDA UDI	Class II	Unknown
Trial Procedure Kit	CPKT-726940-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-107324-0006	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Custom Procedure Kit	4001462	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-107301-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	101995	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.