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 - International Life Sciences

Address:

2252 Northwest Pkwy SE Suite G

MARIETTA

30067

United States

Authorised Representative/ UK Responsible Person
Name: Templar Regulatory Consulting Limited
Address:

11 Amor Way

Letchworth Garden City

Hertfordshire SG61UG

England United Kingdom

Code/Term Type

Extra-gynaecological surgical mesh synthetic polymer bioabsorbable Extra-gynaecological surgical mesh synthetic polymer bioabsorbable Class III

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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