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Meditech Endoscopy Limited

United Kingdom (ex Northern Ireland)·GB-MF-000014143

Last updated May 23, 2026

What Meditech Endoscopy Limited makes

Meditech Endoscopy Limited manufactures reusable device sterilization and disinfection containers, including enzymatic and neutral cleaning systems like StageOne, as well as accessories such as ValveSafe, PrioriTag, Tote Timer, and ColoGrip for endoscopy equipment.

Their portfolio consists of Class I medical devices, all registered in the EU via the eudamed database. The company is based in the United Kingdom.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Meditech Endoscopy Limited manufacture?

Meditech Endoscopy Limited specialises in reusable device sterilisation and disinfection containers. Their portfolio includes systems for enzymatic and neutral cleaning, such as StageOne (Enzymatic) and StageOne (Neutral), as well as accessories like ValveSafe, PrioriTag, Tote Timer, and ColoGrip. These products are designed to support the safe reprocessing of endoscopy equipment.

Where is Meditech Endoscopy Limited based?

Meditech Endoscopy Limited is based in the United Kingdom. The company’s location is relevant for understanding its regulatory framework and compliance with UK and EU medical device regulations.

Which regulatory registries list Meditech Endoscopy Limited’s devices?

Meditech Endoscopy Limited’s devices are listed in the eudamed database, which is the official EU registry for medical devices. This registry ensures transparency and traceability of Class I devices under EU Medical Device Regulation (MDR) or In Vitro Diagnostic Regulation (IVDR).

How are Meditech Endoscopy Limited’s devices classified?

All devices manufactured by Meditech Endoscopy Limited fall under Class I classification. This classification applies to low-risk medical devices, such as reusable sterilisation and disinfection containers, which typically pose minimal risk to patients and users. Classification determines regulatory requirements, and Class I devices generally undergo less stringent scrutiny than higher-risk categories.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United Kingdom (ex Northern Ireland)
Address
Suite 1,, Bowden Terminal, , Basildon, Essex , United Kingdom (ex Northern Ireland)
LinkedIn
—
Facebook
—
Phone
+44 (0)1268 534035
PRRC Contact
Peter Ramsey
EUDAMED SRN
GB-MF-000014143
FDA FEI Number
—
DUNS Number
—

Catalogue (6)

DeviceModel / ReferenceRegistriesClassStatus
ValveSafe INOV8-001
EUDAMED
Class IActive
PrioriTag INOV8-051
EUDAMED
Class IActive
StageOne (Enzymatic) INOV8-009E
EUDAMED
Class IActive
Tote Timer INOV8-048
EUDAMED
Class IActive
ColoGrip INOV8-014
EUDAMED
Class IActive
StageOne (Neutral) INOV8-009
EUDAMED
Class IActive

Related Companies

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Meditech Endoscopy, Ltd. US