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 - Transmed (China) Co. Ltd.

Address:

Room 406 Building 3 Phase 2 Accelerator No.11 Yaogu Avenue Jiangbei New Area

Nanjing

Jiangsu 210032

China

Authorised Representative/ UK Responsible Person
Name: lotus global co ltd
Address:

23 Maine Street

Reading

Reading RG2 6AG

England United Kingdom

Code/Term Type

Flexible endoscopic biopsy forceps single-use Flexible endoscopic biopsy forceps single-use Class IIa

Gastrointestinal endoscopic clip short-term Gastrointestinal endoscopic clip short-term Class IIa

Surgical instrument/endoscope cleaning utensil single-use Surgical instrument/endoscope cleaning utensil single-use Class I

Endoscopic bite block basic single-use Endoscopic bite block basic single-use Class I

Endoscopic biopsy valve single-use Endoscopic biopsy valve 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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Code/Term		Type
Flexible endoscopic biopsy forceps single-use	Flexible endoscopic biopsy forceps single-use	Class IIa
Gastrointestinal endoscopic clip short-term	Gastrointestinal endoscopic clip short-term	Class IIa
Surgical instrument/endoscope cleaning utensil single-use	Surgical instrument/endoscope cleaning utensil single-use	Class I
Endoscopic bite block basic single-use	Endoscopic bite block basic single-use	Class I
Endoscopic biopsy valve single-use	Endoscopic biopsy valve single-use	Class I