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 - Neitz Instruments Co. Ltd.

Address:

4F Ichibancho Court 15-21 Ichibancho

Chiyoda-ku Tokyo

102-0082

Japan

Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Surgical binoculars reusable Surgical binoculars reusable Class I

Retinoscope battery-powered Retinoscope battery-powered Class I

Direct ophthalmoscope Direct ophthalmoscope Class I

Indirect monocular ophthalmoscope electrically-powered Indirect monocular ophthalmoscope electrically-powered Class I

Indirect binocular ophthalmoscope Indirect binocular ophthalmoscope Class I

Head-worn lamp Head-worn lamp 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
Surgical binoculars reusable	Surgical binoculars reusable	Class I
Retinoscope battery-powered	Retinoscope battery-powered	Class I
Direct ophthalmoscope	Direct ophthalmoscope	Class I
Indirect monocular ophthalmoscope electrically-powered	Indirect monocular ophthalmoscope electrically-powered	Class I
Indirect binocular ophthalmoscope	Indirect binocular ophthalmoscope	Class I
Head-worn lamp	Head-worn lamp	Class I