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 - Altaylar Medikal Tibbi Malzemeleri Inaat Tekstil Gida Ithalat Ihracat Sanayi ve Ticaret Ltd. ti.

Address:

Malikoy NH Baskent OSB19 Ankara Turkey 06909 Cadde No 54 Sincan

Malikoy NH BaskentOSB19 Ankara Turkey 06909

Ankara

06909

Turkey

Authorised Representative/ UK Responsible Person
Name: Psephos Limited
Address:

Sussex Innovation Centre Science Park Square

Falmer

Brighton

East Sussex BN1 9SB

England United Kingdom

Code/Term Type

Extra-gynaecological surgical mesh synthetic polymer non-bioabsorbable Extra-gynaecological surgical mesh synthetic polymer non-bioabsorbable Class IIb

Plant polysaccharide haemostatic agent bioabsorbable Plant polysaccharide haemostatic agent bioabsorbable 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
Extra-gynaecological surgical mesh synthetic polymer non-bioabsorbable	Extra-gynaecological surgical mesh synthetic polymer non-bioabsorbable	Class IIb
Plant polysaccharide haemostatic agent bioabsorbable	Plant polysaccharide haemostatic agent bioabsorbable	Class III