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Intermark Medical Innovations Ltd

United Kingdom (ex Northern Ireland)·GB-MF-000007221

Last updated May 23, 2026

What Intermark Medical Innovations Ltd makes

Intermark Medical Innovations Ltd manufactures medical devices for bowel preparation and irrigation, including the Proctowash and Retrowash systems. These devices are designed for use in clinical settings to cleanse the colon prior to procedures or treatments, such as endoscopy or surgery. The portfolio includes both manual and automated irrigation solutions tailored for patient comfort and procedural efficiency.

The company’s devices are classified under EU regulations as Class I and Class IIa, with all relevant products registered in the EU’s eudamed database. These classifications reflect varying levels of risk and regulatory oversight, ensuring compliance with medical device directives. The manufacturer 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 Intermark Medical Innovations Ltd manufacture?

Intermark Medical Innovations Ltd specialises in medical devices for bowel preparation and irrigation. Their portfolio includes systems like the Proctowash and Retrowash, which are designed to cleanse the colon before procedures such as endoscopy or surgery. These devices are intended for clinical use and include both manual and automated irrigation solutions to improve patient comfort and procedural efficiency.

Where is Intermark Medical Innovations Ltd based?

Intermark Medical Innovations Ltd is headquartered in the United Kingdom. The company’s location in the UK aligns with its focus on developing and manufacturing medical devices that comply with European Union regulatory standards.

Which regulatory registries list Intermark Medical Innovations Ltd’s devices?

Intermark Medical Innovations Ltd’s devices are registered in the EU’s eudamed database, which is the official portal for medical device information under EU regulations. This ensures transparency and compliance with the EU’s medical device tracking requirements.

How are Intermark Medical Innovations Ltd’s devices classified under EU regulations?

Intermark Medical Innovations Ltd’s devices are classified as Class I and Class IIa under EU medical device regulations. This classification depends on factors like risk level, intended use, and potential patient exposure. Class I devices pose the lowest risk, while Class IIa devices require additional scrutiny to ensure safety and performance, reflecting their moderate risk profile.

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

Information

Country
United Kingdom (ex Northern Ireland)
Address
34, Southborough Road, Bromley, United Kingdom (ex Northern Ireland)
LinkedIn
—
Facebook
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Phone
—
PRRC Contact
Alan Smith
EUDAMED SRN
GB-MF-000007221
FDA FEI Number
—
DUNS Number
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Catalogue (3)

DeviceModel / ReferenceRegistriesClassStatus
Proctowash PR01
EUDAMED
Class IActive
Retrowash RW35
EUDAMEDFDA UDI
Class IIaActive
Retrowash RW46
EUDAMEDFDA UDI
Class IIaActive

Related Companies

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Importers

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Notified Bodies

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Authorities

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FDA Establishments (1)

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

  • Intermark Medical Innovations Limited US