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 - Cetro Medical AB

Address:

Nitgatan 11

Smalandsstenar

333 33

Sweden

Authorised Representative/ UK Responsible Person
Name: International Associates Limited
Address:

38 Queen Street

Glasgow

G1 3DX

Scotland United Kingdom

Code/Term Type

Arthroscopic obturator Arthroscopic obturator Class IIa

Umbilical cord clamp single-use Umbilical cord clamp single-use Class I

Vaginal speculum single-use Vaginal speculum single-use Class I

Amniotic membrane perforator single-use Amniotic membrane perforator 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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Code/Term		Type
Arthroscopic obturator	Arthroscopic obturator	Class IIa
Umbilical cord clamp single-use	Umbilical cord clamp single-use	Class I
Vaginal speculum single-use	Vaginal speculum single-use	Class I
Amniotic membrane perforator single-use	Amniotic membrane perforator single-use	Class IIa