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 - Traverse Rescue LLC

Address:

Tedlo St

Mississauga

ON L5A 3V3

Canada

Authorised Representative/ UK Responsible Person
Name: Ferno (UK) Limited
Address:

Ferno House Stubs Beck Lane West 26 Industrial Estate

Cleckheaton

West Yorkshire BD19 4TZ

United Kingdom

Code/Term Type

Patient lifting system stretcher Patient lifting system stretcher Class I

Stretcher equipment holder Stretcher equipment holder Class I

General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness Class I

General-purpose patient lifting system sling/harness General-purpose patient lifting system sling/harness 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
Patient lifting system stretcher	Patient lifting system stretcher	Class I
Stretcher equipment holder	Stretcher equipment holder	Class I
General-purpose patient lifting system sling/harness	General-purpose patient lifting system sling/harness	Class I
General-purpose patient lifting system sling/harness	General-purpose patient lifting system sling/harness	Class I