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 - Oasis Medikal Ürünler Kimya Turizm Sanayi ve Tic. A.

Address:

Fatih Mah. 3105. Cad. No:8 Kahramankazan

Ankara

06980

Turkey

Authorised Representative/ UK Responsible Person
Name: Wellspect Ltd
Address:

Stroudwater Business Park Brunel Way

Stonehouse

Stonehouse

Gloucestershire GL10 3GB

England United Kingdom

Code/Term Type

Single-administration urethral drainage catheter Single-administration urethral drainage catheter Class I

Single-administration urethral catheterization kit single-use Single-administration urethral catheterization kit single-use Class I

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
Single-administration urethral drainage catheter	Single-administration urethral drainage catheter	Class I
Single-administration urethral catheterization kit single-use	Single-administration urethral catheterization kit single-use	Class I