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 - Ondine Biomedical Inc.

Address:

#888 - 1100 Melville Street

Vancouver BC

V6E 4A6

Canada

Authorised Representative/ UK Responsible Person
Name: MDSS-UK RP LIMITED
Address:

6 Wilmslow Road Rusholme

Manchester

M14 5TP

England United Kingdom

Code/Term Type

General/multiple surgical laser system beam guide single-use General/multiple surgical laser system beam guide single-use Class IIa

Musculoskeletal/physical therapy laser professional Musculoskeletal/physical therapy laser professional Class IIa

Antiseptic swab Antiseptic swab 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
General/multiple surgical laser system beam guide single-use	General/multiple surgical laser system beam guide single-use	Class IIa
Musculoskeletal/physical therapy laser professional	Musculoskeletal/physical therapy laser professional	Class IIa
Antiseptic swab	Antiseptic swab	Class I