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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 63 of 104

Device	Model / Reference	Registries	Class	Status
Endo Carry-On Procedure Kit	CPK-629000-0001	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4010305	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-107544-0003	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-109902-0004	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-106693-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	102893	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4006510	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	100894	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4010481	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	100970	FDA UDI	Class II	Active
DentaPure 365-Day Municipal Cartridge	DP365M	FDA UDI	Class I	Active
FiberFlo	93022-065	FDA UDI	Class II	Unknown
Endo Carry-On Procedure Kit	CPK-108654-0005	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-597000-0003	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009362	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4006527	FDA UDI	Class II	Active
Custom Procedure Kit	4001605	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4007974	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009854	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-132510-0001	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-200732-0001	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Custom Procedure Kit	CPK-108357-0001	FDA UDI	Class I	Unknown
FiberFlo	93022-161	FDA UDI	Class II	Unknown
Custom procedure Kit	4000987	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	102916	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-103352-0008	FDA UDI	Class I	Unknown
Essential Kit	4000934	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-200169-0002	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009048	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4007872	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4006255	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4007819	FDA UDI	Class II	Active
Custom Procedure Kit	4004337	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009168	FDA UDI	Class II	Active
FiberFlo	93022-152	FDA UDI	Class II	Unknown
Endo Carry-On Procedure Kit	CPK-949400-0001	FDA UDI	Class I	Unknown
Custom Procedure Kit	CPK-107685-0001	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009760	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008086	FDA UDI	Class II	Active
Endogator	100125	FDA UDI	Class II	Unknown
Endo Carry-On Procedure Kit	100804	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-101078-0002	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-103028-0002	FDA UDI	Class I	Unknown
Custom Procedure Kit	4003161	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-105158-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	101939	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-104331-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-100727-0002	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.