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 38 of 104

Device	Model / Reference	Registries	Class	Status
Endo Carry-On Procedure Kit	102924	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-107720-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-834500-0002	FDA UDI	Class II	Active
Custom Procedure Kit	CPK-339347-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-782404-0003	FDA UDI	Class I	Unknown
Custom Procedure Kit	CPK-918616-0001	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4010623	FDA UDI	Class II	Active
Ssd-102	SSD-102	FDA UDI	Class II	Unknown
Custom Procedure Kit	CPK-103773-0023	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-200395-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-819200-0001	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	100896	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-205350-0002	FDA UDI	Class I	Unknown
Custom Procedure Kit	4003327	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009189	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-103138-0001	FDA UDI	Class II	Active
Custom Procedure Kit	4000587	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-103974-0003	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009912	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4007400	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-101695-0002	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	100835	FDA UDI	Class I	Unknown
Custom Procedure Kit	4000101	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4007735	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-103793-0002	FDA UDI	Class I	Unknown
Renasol Acid Concentrate	SB-1063	FDA UDI	Class II	Unknown
Endo Carry-On Procedure Kit	CPK-104641-0009	FDA UDI	Class II	Active
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Custom Procedure Kit	4003534	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009698	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-821400-0001	FDA UDI	Class I	Unknown
Trial Procedure Kit	CPKT-104641-0003	FDA UDI	Class I	Unknown
Custom Procedure Kit	CPK-200104-0008	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPKT-109774-0001-33	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-104258-0003	FDA UDI	Class I	Unknown
Trial Procedure Kit	CPKT-107946-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-104196-0002	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-110582-0001	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4008941	FDA UDI	Class II	Active
Custom Procedure Kit	4002617	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008885	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4009007	FDA UDI	Class II	Active
Custom Procedure Kit	4002620	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-107330-0002	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Endo Carry-On Procedure Kit	CPK-104003-0001	FDA UDI	Class I	Unknown
Impervious Gown	200352	FDA UDI	Class I	Active
Custom Procedure Kit	CPK-103773-0040	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.