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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 31 of 104

Device	Model / Reference	Registries	Class	Status
Endo-Carry-on Procedure Kit	4007405	FDA UDI	Class II	Active
DentaPure 365-Day Independent Water Bottle Cartridge	DP365B	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009209	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	100846	FDA UDI	Class II	Active
Custom Procedure Kit	4000125	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPKT-103773-0005	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4008357	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009911	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4006250	FDA UDI	Class II	Active
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Endo Carry-on Custom Procedure Kit	4005903	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-108565-0002	FDA UDI	Class I	Unknown
Centrisol Acid Concentrate	SB-330	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-844500-0005	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Custom Procedure Kit	4003314	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4006063	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-101048-0005	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009730	FDA UDI	Class II	Active
Custom Procedure Kit	CPK-103773-0046	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-200303-0001	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-107516-0004	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4006222	FDA UDI	Class II	Active
Custom Procedure Kit	4001008	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-106941-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-491013-0010	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-102656-0001	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009158	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009165	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-100759-0001	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4010482	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-108290-0001	FDA UDI	Class I	Unknown
Centrisol Acid Concentrate	SB-130	FDA UDI	Class II	Unknown
Endo Carry-On Procedure Kit	CPK-110557-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-200843-0003	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-104750-0003	FDA UDI	Class I	Unknown
Custom Procedure Kit	4000031	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	100985	FDA UDI	Class I	Unknown
EndoGator Hybrid	4003180	FDA UDI	Class II	Active
Custom Procedure Kit	4001007	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-102688-0003	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009739	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4010676	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009279	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009510	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	100840	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-200529-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-665500-0001	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	102837	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.