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

Back to MHRA

Manufacturer's Devices - Kem Enterprises Inc.

Address:

KEM Enterprises Inc. 579 Roundtree Drive NE

ADA Michigan 49301

Michigan

49301

United States

Authorised Representative/ UK Responsible Person
Name: Respond Healthcare limited
Address:

Greypoint Cardiff Business park

LLanishen

Cardiff

Cardiff Cf14 5WF

United Kingdom

Code/Term Type

Ostomy bag pressure release valve Ostomy bag pressure release valve 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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