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 - WomanCare Global

Address:

1640 Roanoke Blvd.

Salem

VA 24153

United States

Authorised Representative/ UK Responsible Person
Name: Donawa Lifescience Ltd
Address:

Aviation Business Park Enterprise Close

Christchurch

BH23 6NX

England United Kingdom

Code/Term Type

Intrauterine cannula single-use Intrauterine cannula single-use Class I

Fixed-diameter cervical dilator single-use Fixed-diameter cervical dilator single-use Class I

Abortion suction system manual aspirator Abortion suction system manual aspirator Class I

Abortion suction system manual aspirator Abortion suction system manual aspirator 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
Intrauterine cannula single-use	Intrauterine cannula single-use	Class I
Fixed-diameter cervical dilator single-use	Fixed-diameter cervical dilator single-use	Class I
Abortion suction system manual aspirator	Abortion suction system manual aspirator	Class I
Abortion suction system manual aspirator	Abortion suction system manual aspirator	Class I