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Farla Medical Ltd

United Kingdom (ex Northern Ireland)·GB-MF-000003751

Last updated May 23, 2026

What Farla Medical Ltd makes

Farla Medical Ltd manufactures lubricating and preparation solutions for medical procedures, including products like MediLube, which are designed for use in clinical settings. Their portfolio also includes devices under the Instramed brand, which appear to be related to medical instrumentation or accessories for diagnostic or procedural use.

The company’s products are classified under EU medical device regulations as Class I and Class IIa, and they are registered in the EU’s eudamed database. Farla Medical Ltd 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 Farla Medical Ltd manufacture?

Farla Medical Ltd specialises in lubricating and preparation solutions for medical procedures. Their portfolio includes products like MediLube, which are intended for clinical use, as well as devices under the Instramed brand, which appear to serve as accessories or instrumentation for diagnostic or procedural applications. These products are designed to support medical professionals in ensuring smooth and safe procedures.

Where is Farla Medical Ltd based?

Farla Medical Ltd is based in the United Kingdom. This location places them within the EU regulatory framework, which governs the classification and compliance requirements for their medical devices.

Which regulatory registries list Farla Medical Ltd’s devices?

Farla Medical Ltd’s devices are listed in the eudamed database, the official EU registry for medical devices. This registration ensures transparency and compliance with EU medical device regulations, allowing healthcare professionals and authorities to verify the company’s products.

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

Farla Medical Ltd’s devices fall under Class I and Class IIa classifications in the EU. Class I devices are generally low-risk, such as lubricating solutions, while Class IIa devices involve a slightly higher risk, often requiring additional measures to ensure safety and performance. The classification determines the regulatory requirements for manufacturing, testing, and compliance.

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

Information

Country
United Kingdom (ex Northern Ireland)
Address
Unit 2, Staples Corner Business Park , London , United Kingdom (ex Northern Ireland)
LinkedIn
—
Facebook
—
Phone
0345 193 5 193
PRRC Contact
Ash Puri
EUDAMED SRN
GB-MF-000003751
FDA FEI Number
—
DUNS Number
—

Catalogue (5)

DeviceModel / ReferenceRegistriesClassStatus
Instramed S42-9567
EUDAMED
Class IActive
Farla Medical S42-2222
EUDAMED
Class IActive
Instramed S42-2362
EUDAMED
Class IActive
Instramed S42-9105
EUDAMED
Class IActive
MediLube 6635
EUDAMED
Class IIaActive

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