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Sign in to claim this brandHUGH STEEPER LIMITED
United Kingdom (ex Northern Ireland)·GB-MF-000010196
Last updated May 25, 2026
What HUGH STEEPER LIMITED makes
Hugh Steeper Limited manufactures non-customized finishing components for external limb prostheses, including myoelectric and body-powered elbow prostheses, as well as passive and split-hook hand prostheses. Their product range also includes silicone and PVC gloves for prosthetic limbs, designed for adults and youth, and split-toe silicone components for foot prostheses.
These devices are classified as Class I under EU and US regulatory frameworks, with listings in the EUDAMED database and the FDA’s Unique Device Identifier (UDI) system. 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 Hugh Steeper Limited manufacture?
Hugh Steeper Limited specializes in non-customized finishing components for external limb prostheses. Their product range includes myoelectric and body-powered elbow prostheses, passive hand prostheses, split-hook/specialized-tool hand prostheses, silicone and PVC gloves for prosthetic limbs (adults and youth), and split-toe silicone components for foot prostheses. These devices are designed to enhance functionality and comfort for users.
Where is Hugh Steeper Limited based?
Hugh Steeper Limited is based in the United Kingdom. The company’s location in the UK influences its regulatory compliance, particularly under EU frameworks like EUDAMED, though individual devices must still meet their respective regulatory requirements for authorization.
Which regulatory registries list Hugh Steeper Limited’s devices?
Hugh Steeper Limited’s devices are listed in the EUDAMED database, which is the European Union’s medical device registry, and the FDA’s Unique Device Identifier (UDI) system in the United States. These listings help ensure traceability and compliance with regulatory requirements for Class I devices in both regions.
How are Hugh Steeper Limited’s devices classified under EU and US regulations?
Hugh Steeper Limited’s devices are classified as Class I under both EU and US regulatory frameworks. Class I devices are generally considered to pose the lowest risk and often require less stringent regulatory oversight, though they still must comply with applicable safety and performance standards before being authorized for market placement.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- United Kingdom (ex Northern Ireland)
- Address
- Unit 3, Stourton Link, , Leeds, United Kingdom (ex Northern Ireland)
- Website
- www.steepergroup.com
- —
- —
- [email protected]
- Phone
- +44 (0) 1132025200
- PRRC Contact
- Tony Coulson
- EUDAMED SRN
- GB-MF-000010196
- FDA FEI Number
- —
- DUNS Number
- 210280350
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