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 - PROCEPT BioRobotics Corporation

Address:

900 ISLAND DRIVE

Redwood City

California 94065

United States

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

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Patient surgical drape single-use Patient surgical drape single-use Class I

Water jet knife system Water jet knife system Class IIb

Water jet knife system handpiece single-use Water jet knife system handpiece single-use Class IIa

Rigid endoscope telescope Rigid endoscope telescope Class IIa

Rigid endoscope telescope Rigid endoscope telescope Class IIb

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
Patient surgical drape single-use	Patient surgical drape single-use	Class I
Water jet knife system	Water jet knife system	Class IIb
Water jet knife system handpiece single-use	Water jet knife system handpiece single-use	Class IIa
Rigid endoscope telescope	Rigid endoscope telescope	Class IIa
Rigid endoscope telescope	Rigid endoscope telescope	Class IIb