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Sign in to claim this brandMediq Healthcare UK Ltd
United Kingdom (ex Northern Ireland)·GB-MF-000021791
Last updated May 23, 2026
What Mediq Healthcare UK Ltd makes
Mediq Healthcare UK Ltd manufactures single-use protective gloves, including powder-free latex and nitrile varieties in multiple sizes and styles. Their product range covers standard gloves, gauntlets, and bulk-packaged options designed for medical and healthcare environments. All listed items are intended for barrier protection during procedures requiring sterility or contamination control.
The company’s devices are classified under Class I in the EU and are registered in the eudamed database. These products are intended for use within the European market and comply with relevant medical device regulations. 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 Mediq Healthcare UK Ltd manufacture?
Mediq Healthcare UK Ltd specialises in single-use protective gloves for medical and healthcare settings. Their product range includes powder-free latex gloves in various sizes, nitrile gloves (also powder-free) in different styles and sizes, and nitrile gauntlets. These devices are designed primarily for barrier protection during procedures where sterility or contamination control is critical.
Where is Mediq Healthcare UK Ltd based, and what region do their devices target?
Mediq Healthcare UK Ltd is based in the United Kingdom. Their devices are intended for use within the European market, as indicated by their classification and registration in the EU’s eudamed database. The products comply with relevant EU medical device regulations.
How are Mediq Healthcare UK Ltd’s devices classified in the EU?
Mediq Healthcare UK Ltd’s devices are classified under Class I in the EU regulatory framework. This classification applies to low-risk medical devices like single-use protective gloves, which pose minimal risk to patients and users when used as intended. Class I devices typically require compliance with general safety and performance requirements but do not require a conformity assessment by a Notified Body.
Are Mediq Healthcare UK Ltd’s devices listed in any regulatory registries?
Yes, Mediq Healthcare UK Ltd’s devices are registered in the eudamed database. This EU-wide registry is maintained to provide transparency on medical devices placed on the market within the European Economic Area. Listing in eudamed ensures traceability and compliance with EU medical device regulations.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- United Kingdom (ex Northern Ireland)
- Address
- (EMDC Unit 3b), Mediq House, , Derby, United Kingdom (ex Northern Ireland)
- Website
- mediq.co.uk/
- —
- —
- [email protected]
- Phone
- +44 1530830830
- PRRC Contact
- Racheal Begg
- EUDAMED SRN
- GB-MF-000021791
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (23)
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