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

Back to MHRA

Manufacturer's Devices - Su Biyomedikal Sistemler ve Saglik Hizmetleri San ve Tic A.S

Address:

Orhangazi Mah. 1673 Sok

Istanbul

Essenyurt 34538

Turkey

Authorised Representative/ UK Responsible Person
Name: Reflex Medical Limited
Address:

The Blue Tower Townsend

Shepton Mallet

Somerset BA4 5SB

England United Kingdom

Code/Term Type

General surgical procedure kit non-medicated single-use General surgical procedure kit non-medicated single-use Class IIa

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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