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 - CHA Meditech Co. Ltd.

Address:

#102 103 204 Migun Techno World I 199 Techno 2-ro Yuseong-gu

Daejeon

34025

South Korea

Authorised Representative/ UK Responsible Person
Name: Emergo Consulting (UK) Limited
Address:

Compass House Vision Park Histon c/o Cr360 – UL International

Cambridge

CB24 9BZ

England United Kingdom

Code/Term Type

Surgical anti-adhesion material implantable bioabsorbable non-medicated Surgical anti-adhesion material implantable bioabsorbable non-medicated Class III

Dermal tissue reconstructive material microbe-derived anaesthetic Dermal tissue reconstructive material microbe-derived anaesthetic Class III

Dermal tissue reconstructive material microbe-derived Dermal tissue reconstructive material microbe-derived 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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Code/Term		Type
Surgical anti-adhesion material implantable bioabsorbable non-medicated	Surgical anti-adhesion material implantable bioabsorbable non-medicated	Class III
Dermal tissue reconstructive material microbe-derived anaesthetic	Dermal tissue reconstructive material microbe-derived anaesthetic	Class III
Dermal tissue reconstructive material microbe-derived	Dermal tissue reconstructive material microbe-derived	Class III