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 - Gynemed GmbH & Co. KG

Address:

Lübecker Straße 9

Lensahn

23738

Germany

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

110 Windmill Road

Sunbury-on-Thames

Middlesex TW16 7HD

United Kingdom

Code/Term Type

IVF medium IVF medium Class IIb

IVF oocyte aspiration needle single-use IVF oocyte aspiration needle single-use Class IIa

Assisted reproduction microtool Assisted reproduction microtool Class IIa

IVF medium kit IVF medium kit Class IIa

User-induced micropipette User-induced micropipette Class III

Cell culture medium IVD Cell culture medium IVD Class III

Cell culture medium IVD Cell culture medium IVD Class IIa

Cell culture medium IVD Cell culture medium IVD IVD General

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
IVF medium	IVF medium	Class IIb
IVF oocyte aspiration needle single-use	IVF oocyte aspiration needle single-use	Class IIa
Assisted reproduction microtool	Assisted reproduction microtool	Class IIa
IVF medium kit	IVF medium kit	Class IIa
User-induced micropipette	User-induced micropipette	Class III
Cell culture medium IVD	Cell culture medium IVD	Class III
Cell culture medium IVD	Cell culture medium IVD	Class IIa
Cell culture medium IVD	Cell culture medium IVD	IVD General