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 - YTY Industry Sdn Bhd

Address:

Lot 1422-1424 Batu 10 Lekr

Sitiawan

Perak Darul Ridzuan 32020

Malaysia

Authorised Representative/ UK Responsible Person
Name: Amstermed UK Ltd
Address:

Unit 109 - 54 Bloomfied Avenue

Belfast

BT5 5AD

Northern Ireland United Kingdom

Code/Term Type

Nitrile examination/treatment glove non-powdered non-antimicrobial Nitrile examination/treatment glove non-powdered non-antimicrobial 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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