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 - Apollo Rubber Sdn Bhd

Address:

Lot PT 609 Lorong Perak 3

Telok Panglima Garang Industrial Estate Telok Panglima Garang

Selangor

Telok Panglima Garang 42500

Malaysia

Authorised Representative/ UK Responsible Person
Name: ALS International Ltd Trading as I3CGLOBAL(UK)
Address:

Office 54 58 Peregrine Road

Hainault

Ilford

Essex IG6 3SZ

England United Kingdom

Code/Term Type

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

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