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 - American Diagnostic Corporation

Address:

55 Commerce Drive

Hauppauge

NY 11788

United States

Authorised Representative/ UK Responsible Person
Name: Vera Global Ltd
Address:

86-90 Paul Street 3rd Floor

London

EC2A 4NE

England United Kingdom

Code/Term Type

Fixed examination/treatment room light Fixed examination/treatment room light Class I

Mechanical stethoscope Mechanical stethoscope Class I

Dermatoscope optical Dermatoscope optical Class I

Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Class I

Direct ophthalmoscope Direct ophthalmoscope Class I

Otoscope direct Otoscope direct Class I

Ophthalmic/otologic diagnostic set Ophthalmic/otologic diagnostic set Class I

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

© 2011 Crown Copyright. To contact us about this website, use our feedback form.

Code/Term		Type
Fixed examination/treatment room light	Fixed examination/treatment room light	Class I
Mechanical stethoscope	Mechanical stethoscope	Class I
Dermatoscope optical	Dermatoscope optical	Class I
Aneroid manual sphygmomanometer	Aneroid manual sphygmomanometer	Class I
Direct ophthalmoscope	Direct ophthalmoscope	Class I
Otoscope direct	Otoscope direct	Class I
Ophthalmic/otologic diagnostic set	Ophthalmic/otologic diagnostic set	Class I