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

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Manufacturer's Devices - Nemaura Pharma

Address:

5 Oakwood Drive Loughborough University Science and Enterprise Park 5 Oakwood Drive

Loughborough

Leicestershire LE11 3QF

United Kingdom

Authorised Representative/ UK Responsible Person
Name: Not Available

Address:

Code/Term Type

Noninvasive interstitial-fluid glucose monitoring device Noninvasive interstitial-fluid glucose monitoring device Class I

Surgical Instruments (Re-Usable And Non-Powered) Surgical Instruments (Re-Usable And Non-Powered) Class I

Surgical Instruments (Re-Usable And Non-Powered) Surgical Instruments (Re-Usable And Non-Powered) Class IIb

Surgical Instruments (Re-Usable And Non-Powered) Surgical Instruments (Re-Usable And Non-Powered) 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
Noninvasive interstitial-fluid glucose monitoring device	Noninvasive interstitial-fluid glucose monitoring device	Class I
Surgical Instruments (Re-Usable And Non-Powered)	Surgical Instruments (Re-Usable And Non-Powered)	Class I
Surgical Instruments (Re-Usable And Non-Powered)	Surgical Instruments (Re-Usable And Non-Powered)	Class IIb
Surgical Instruments (Re-Usable And Non-Powered)	Surgical Instruments (Re-Usable And Non-Powered)	Class I