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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 62 of 104

Device	Model / Reference	Registries	Class	Status
Endo Carry-On Procedure Kit	CPK-238500-0013	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4008163	FDA UDI	Class II	Active
Custom Procedure Kit	4005669	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	101805	FDA UDI	Class II	Active
Endo Smartcap	100150CO2	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	100861	FDA UDI	Class I	Unknown
Intercept Wipes	ML02-0107	FDA UDI	Class I	Active
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Custom Procedure Kit	CPK-106655-0001	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4010533	FDA UDI	Class II	Active
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Custom Procedure Kit	4000086	FDA UDI	Class II	Active
Custom Procedure Kit	4000202	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-104702-0005	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-205350-0003	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Endo Carry-On Procedure Kit	CPK-103880-0001	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4008084	FDA UDI	Class II	Active
Custom Procedure Kit	4002618	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-100727-0006	FDA UDI	Class I	Unknown
Custom Procedure Kit	CPK-103986-0001	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009500	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4010557	FDA UDI	Class II	Active
Scope Buddy Plus Blanking Cap	SB110HU1017	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-200233-0002	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-108349-0004	FDA UDI	Class I	Unknown
Trial Procedure Kit	CPKT-457000-0002	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4001457	FDA UDI	Class II	Active
Custom Procedure Kit	4005661	FDA UDI	Class II	Active
Custom Procedure Kit	4001441	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-107638-0001	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009065	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-105070-0001	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4008137	FDA UDI	Class II	Active
Custom Procedure Kit	4003151	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008883	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-101215-0004	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-102292-0002	FDA UDI	Class II	Active
Defendo	Defendo Fujifilm 700 Series	FDA UDI	Class II	Active
Custom Procedure Kit	4000404	FDA UDI	Class II	Active
Essential Kit	4000926	FDA UDI	Class II	Active
Custom Procedure Kit	4000274	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-102761-0001	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4008335	FDA UDI	Class II	Active
ENDOGATOR Kit	100626	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009733	FDA UDI	Class II	Active
Custom Procedure Kit	4002369	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-100746-0001	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4007881	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.