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 - TAN SIN LIAN INDUSTRIES SDN. BHD.

Address:

No. 1-14 Jalan Indah 2 Taman Indah Jalan Haji Abdullah

Muar

Johor 84000

Malaysia

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

Sandford Gate East Point Business Park

Oxford

OX4 6LB

England United Kingdom

Code/Term Type

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

Hevea-latex examination/treatment glove non-powdered non-antimicrobial Hevea-latex examination/treatment glove non-powdered non-antimicrobial Class I

Hevea-latex examination/treatment glove powdered Hevea-latex examination/treatment glove powdered 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
Nitrile examination/treatment glove non-powdered non-antimicrobial	Nitrile examination/treatment glove non-powdered non-antimicrobial	Class I
Hevea-latex examination/treatment glove non-powdered non-antimicrobial	Hevea-latex examination/treatment glove non-powdered non-antimicrobial	Class I
Hevea-latex examination/treatment glove powdered	Hevea-latex examination/treatment glove powdered	Class I