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 48 of 104

Device	Model / Reference	Registries	Class	Status
FiberFlo	93250-192	FDA UDI	Class II	Unknown
Endo Carry-On Procedure Kit	102884	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-110968-0001	FDA UDI	Class I	Unknown
Endogator	100115	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-103225-0003	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009476	FDA UDI	Class II	Active
Custom Procedure Kit	CPK-101276-0006	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008041	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-108984-0003	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-663055-0001	FDA UDI	Class I	Unknown
ENDOGATOR hybrid irrigation tubing	100605B	FDA UDI	Class II	Active
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009157	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009004	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-101048-0006	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-105655-0002	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-101241-0003	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	102811	FDA UDI	Class I	Unknown
Pull Thru W/ Stubby Combo Single	4002593	FDA UDI	Class I	Active
Endo Carry-On Procedure Kit	CPK-107464-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-867500-0002	FDA UDI	Class I	Unknown
Custom Procedure Kit	4001855	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009361	FDA UDI	Class II	Active
Custom Procedure Kit	4000250	FDA UDI	Class II	Active
DentaPure 365-Day Independent Water Bottle Cartridge	DPI365B	FDA UDI	Class I	Active
Preclean Kit	4000899	FDA UDI	Class II	Active
Custom Procedure Kit	4000529	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Endo Carry-on Procedure Kit	4009291	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009088	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008820	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4010032	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-104344-0001	FDA UDI	Class I	Unknown
Custom Procedure Kit	CPK-103773-0037	FDA UDI	Class I	Unknown
FiberFlo	93022-056	FDA UDI	Class II	Unknown
Endo Carry-on Procedure Kit	4010046	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4007514	FDA UDI	Class II	Active
Minncare HD	3029764	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-103352-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-530095-0001	FDA UDI	Class I	Unknown
ENDOGATOR Kit	100603	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-106694-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-103225-0002	FDA UDI	Class I	Unknown
Preclean Kit	4000901	FDA UDI	Class II	Active
Custom Procedure Kit	4000089	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4008974	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4007734	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-491013-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-618000-0001	FDA UDI	Class I	Unknown
Custom Procedure Kit	4004193	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.