Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

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Manufacturer's Devices - Epimed International Inc.

Address:

13958 Diplomat Drive

Dallas

Texas 75234

United States

Authorised Representative/ UK Responsible Person
Name: Emergo Consulting (UK) Limited
Address:

Compass House Vision Park Histon c/o Cr360 – UL International

Cambridge

CB24 9BZ

England United Kingdom

Code/Term Type

Epidural needle non-threaded Epidural needle non-threaded Class IIa

Epidural anaesthesia set non-medicated Epidural anaesthesia set non-medicated Class IIa

Peripheral nerve-block blunt needle Peripheral nerve-block blunt needle Class IIa

Percutaneous radio-frequency ablation probe cannula single-use Percutaneous radio-frequency ablation probe cannula single-use Class IIa

Peripheral nerve-block blunt needle access cannula Peripheral nerve-block blunt needle access cannula Class IIa

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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Code/Term		Type
Epidural needle non-threaded	Epidural needle non-threaded	Class IIa
Epidural anaesthesia set non-medicated	Epidural anaesthesia set non-medicated	Class IIa
Peripheral nerve-block blunt needle	Peripheral nerve-block blunt needle	Class IIa
Percutaneous radio-frequency ablation probe cannula single-use	Percutaneous radio-frequency ablation probe cannula single-use	Class IIa
Peripheral nerve-block blunt needle access cannula	Peripheral nerve-block blunt needle access cannula	Class IIa