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 Diskectomy system percutaneous automatic-Diskectomy system percutaneous automatic
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Manufacturer
Address
Authorised Representative
Address
Date Registered
MHRA Reference Number
Stryker Instruments a division of Stryker Corporation
4100 E. Milham Ave
Kalamazoo
Michigan 49001
United States
Stryker UK Ltd
Stryker House Hambridge Road
Newbury
Berkshire RG14 5AW
England United Kingdom
03/03/2021
12472