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 - DHEF INC.

Address:

15F No. 104 & 106 Hsin Tai Wu Rd. Sec. 1 Hsi Chih Dist.

New Taipei City

22441

Taiwan

Authorised Representative/ UK Responsible Person
Name: Insyzor Consulting Ltd
Address:

6 BADMINTON COURT

YATE

BS37 5HZ

England United Kingdom

Code/Term Type

Medical equipment drape single-use Medical equipment drape single-use Class I

Dental matrix band single-use Dental matrix band single-use Class I

X-ray image intensifier X-ray image intensifier 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
Medical equipment drape single-use	Medical equipment drape single-use	Class I
Dental matrix band single-use	Dental matrix band single-use	Class I
X-ray image intensifier	X-ray image intensifier	Class I