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 - Spierings Orthopaedics BV

Address:

Madoerastraat 24

Nijmegen

Gelderland 6524 LH

Netherlands

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

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Bone-resection orthopaedic reamer reusable Bone-resection orthopaedic reamer reusable Class I

Bone trephine Bone trephine Class I

Manual bone mill Manual bone mill Class I

Orthopaedic prosthesis implantation positioning instrument reusable Orthopaedic prosthesis implantation positioning instrument reusable Class I

Extra-gynaecological surgical mesh metal Extra-gynaecological surgical mesh metal Class IIb

Gelatin orthopaedic cement restrictor Gelatin orthopaedic cement restrictor Class III

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
Bone-resection orthopaedic reamer reusable	Bone-resection orthopaedic reamer reusable	Class I
Bone trephine	Bone trephine	Class I
Manual bone mill	Manual bone mill	Class I
Orthopaedic prosthesis implantation positioning instrument reusable	Orthopaedic prosthesis implantation positioning instrument reusable	Class I
Extra-gynaecological surgical mesh metal	Extra-gynaecological surgical mesh metal	Class IIb
Gelatin orthopaedic cement restrictor	Gelatin orthopaedic cement restrictor	Class III