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 - Bio Med Sciences Inc.

Address:

999 Postal Road Allentown PA

Allentown

18109

United States

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

Compass House Vision Park Histon c/o Cr360 – UL International

Cambridge

CB24 9BZ

England United Kingdom

Code/Term Type

Scar management dressing reusable Scar management dressing reusable Class I

Wound-nonadherent dressing permeable non-antimicrobial Wound-nonadherent dressing permeable non-antimicrobial Class IIa

Synthetic polymer semi-permeable film dressing wound-nonadherent Synthetic polymer semi-permeable film dressing wound-nonadherent Class IIa

Wound-nonadherent dressing absorbent non-antimicrobial Wound-nonadherent dressing absorbent non-antimicrobial Class IIa

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
Scar management dressing reusable	Scar management dressing reusable	Class I
Wound-nonadherent dressing permeable non-antimicrobial	Wound-nonadherent dressing permeable non-antimicrobial	Class IIa
Synthetic polymer semi-permeable film dressing wound-nonadherent	Synthetic polymer semi-permeable film dressing wound-nonadherent	Class IIa
Wound-nonadherent dressing absorbent non-antimicrobial	Wound-nonadherent dressing absorbent non-antimicrobial	Class IIa