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 - FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH,,,,,,,,,,,
Address:
Prager Ring 70,,,,,,,,,,,
Aachen,,,,,,,,,,,
52070,,,,,,,,,,,
Germany
Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:
49 Greek Street
London
W1D 4EG
England United Kingdom
Code/Term
Type
Urological surgical procedure kit non-medicated reusable
Urological surgical procedure kit non-medicated reusable
Class I
Extra-gynaecological surgical mesh synthetic polymer non-bioabsorbable
Extra-gynaecological surgical mesh synthetic polymer non-bioabsorbable
Class IIb
Hiatal hernia surgical mesh synthetic polymer non-bioabsorbable
Hiatal hernia surgical mesh synthetic polymer non-bioabsorbable
Class IIb
Female stress urinary incontinence surgical mesh-sling synthetic polymer
Female stress urinary incontinence surgical mesh-sling synthetic polymer
Class IIb
Male stress urinary incontinence surgical mesh-sling synthetic polymer
Male stress urinary incontinence surgical mesh-sling synthetic polymer
Class IIb
Pelvic organ prolapse surgical mesh synthetic polymer
Pelvic organ prolapse surgical mesh synthetic polymer
Class IIb