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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 70 of 104

Device	Model / Reference	Registries	Class	Status
Trial Procedure Kit	CPKT-200169-0003	FDA UDI	Class I	Unknown
Trial Procedure Kit	CPKT-101512-0001	FDA UDI	Class I	Unknown
Double Ended Stubby Brush (180)	4002611	FDA UDI	Class I	Active
Essential Kit	4000936	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009514	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	102835	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4006223	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009162	FDA UDI	Class II	Active
Scope Buddy Plus Tubing	SB-110-HU1011	FDA UDI	Class II	Active
Medivators Hookup	Hookup	FDA UDI	Class II	Unknown
Endo-Carry-on Procedure Kit	4001447	FDA UDI	Class II	Active
Custom Procedure Kit	4003138	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-108349-0002	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009371	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-668000-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-200404-0003	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-105142-0001	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4008811	FDA UDI	Class II	Active
Endo Carry-on Procedure Kit	4009030	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-110619-0001	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Custom Procedure Kit	4001472	FDA UDI	Class II	Active
Custom Procedure Kit	4000194	FDA UDI	Class II	Active
Custom Procedure Kit	4000029	FDA UDI	Class I	Unknown
Endo-Carry-on Procedure Kit	4006561	FDA UDI	Class II	Active
Custom Procedure Kit	4000948	FDA UDI	Class I	Unknown
Medivators Hookup	Hookup	FDA UDI	Class II	Active
Custom Procedure Kit	4004146	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-101215-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-105463-0003	FDA UDI	Class II	Active
Trial Procedure Kit	CPKT-111289-0003	FDA UDI	Class I	Unknown
Trial Procedure Kit	CPKT-107464-0001	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009142	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008022	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	101882	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4007985	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPKT-103604-0001	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPKT-583400-0001	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009352	FDA UDI	Class II	Active
Custom Procedure Kit	CPK-200104-0010	FDA UDI	Class I	Unknown
Endo Carry-On Procedure Kit	CPK-104641-0006	FDA UDI	Class I	Unknown
Renasol Acid Concentrate	SB-1020	FDA UDI	Class II	Unknown
Endo Carry-on Procedure Kit	4010063	FDA UDI	Class II	Active
Custom Procedure Kit	CPK-104330-0003	FDA UDI	Class I	Unknown
Custom Procedure Kit	4003745	FDA UDI	Class II	Active
Endo Carry-On Procedure Kit	CPK-104232-0009	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4009813	FDA UDI	Class II	Active
Endo-Carry-on Procedure Kit	4008756	FDA UDI	Class II	Active
Custom Procedure Kit	4002538	FDA UDI	Class I	Unknown
Endo Carry-on Procedure Kit	4010191	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.