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 - Tarry Medical Products Inc

Address:

22 Shelter Rock Lane

Danbury

Connecticut 06810

United States

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

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Non-respiratory device ambient air filter Non-respiratory device ambient air filter Class I

Flotation therapy bed neonatal Flotation therapy bed neonatal Class I

Infant-hammock bed mattress overlay Infant-hammock bed mattress overlay Class I

Neonatal positioning/nesting device Neonatal positioning/nesting device Class I

Arm procedure positioner single-use Arm procedure positioner 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
Non-respiratory device ambient air filter	Non-respiratory device ambient air filter	Class I
Flotation therapy bed neonatal	Flotation therapy bed neonatal	Class I
Infant-hammock bed mattress overlay	Infant-hammock bed mattress overlay	Class I
Neonatal positioning/nesting device	Neonatal positioning/nesting device	Class I
Arm procedure positioner single-use	Arm procedure positioner single-use	Class I