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 - QUESTALPHA GmbH & Co. KG

Address:

Im Heerfeld 7

Eschenburg

35713

Germany

Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Intranasal splint non-biodegradable Intranasal splint non-biodegradable Class IIb

Ophthalmic sponge Ophthalmic sponge Class I

Surgical scrub sponge Surgical scrub sponge Class I

Surgical scrub sponge Surgical scrub sponge Class IIb

Surgical scrub sponge Surgical scrub sponge Class I

Surgical scrub sponge Surgical scrub sponge Class IIb

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
Intranasal splint non-biodegradable	Intranasal splint non-biodegradable	Class IIb
Ophthalmic sponge	Ophthalmic sponge	Class I
Surgical scrub sponge	Surgical scrub sponge	Class I
Surgical scrub sponge	Surgical scrub sponge	Class IIb
Surgical scrub sponge	Surgical scrub sponge	Class I
Surgical scrub sponge	Surgical scrub sponge	Class IIb