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 - Humeca BV

Address:

Oostermaat 5

Borne

7623 CS

Netherlands

Authorised Representative/ UK Responsible Person
Name: Eurosurgical Ltd
Address:

Merrow Business Park

Guildford

Guildford

Surrey GU4 7WA

England United Kingdom

Code/Term Type

Dermatome blade single-use Dermatome blade single-use Class IIa

Skin graft carrier Skin graft carrier Class I

Woven gauze pad Woven gauze pad Class I

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
Dermatome blade single-use	Dermatome blade single-use	Class IIa
Skin graft carrier	Skin graft carrier	Class I
Woven gauze pad	Woven gauze pad	Class I