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 - The Standard Co Ltd

Address:

Gunpocheomdansaneop 2-Ro

Gunpocheomdansaneop 2-Ro Gunpo-Si

Gyeonggi-Do

Gunpo-Si 15880

South Korea

Authorised Representative/ UK Responsible Person
Name: Omnimed Limited
Address:

Unit 1A Abbas Business Centre Itchen Abbas

Winchester

Hampshire SO21 1BQ

England United Kingdom

Code/Term Type

Tissue marking ink Tissue marking ink Class IIb

Submucosal lift solution/gel Submucosal lift solution/gel Class IIb

Endoscope lens cleaner gas/fluid single-use Endoscope lens cleaner gas/fluid single-use

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
Tissue marking ink	Tissue marking ink	Class IIb
Submucosal lift solution/gel	Submucosal lift solution/gel	Class IIb
Endoscope lens cleaner gas/fluid single-use	Endoscope lens cleaner gas/fluid single-use