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.
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Manufacturer's By Device Filiform urethral bougie-Filiform urethral bougie
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Manufacturer
Address
Authorised Representative
Address
Date Registered
MHRA Reference Number
STEMA Medizintechnik GmbH
take-off GewerbePark 74
Neuhausen ob Eck
78579
Germany
Compliance Solutions (Lifesciences) Ltd
Suite 10 Dunswood House 1 Dunswood Road
Cumbernauld
Glasgow
G67 3EN
United Kingdom
07/20/2021
16098