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 - GMMI SDN. BHD.

Address:

No 12 Persiaran Industri Rapat Perindustrian Ringan Sri Rapat

Ipoh

Perak 31350

Malaysia

Authorised Representative/ UK Responsible Person
Name: P3 Medical Ltd
Address:

Unit 1 Newbridge Close

Newbridge Trading Estate

Bristol

BS4 4AX

England United Kingdom

Code/Term Type

Endotracheal tube introducer single-use Endotracheal tube introducer single-use 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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