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 - Vycor Medical Inc.

Address:

951 Broken Sound Parkway Suite 320

Boca Raton

Florida FL 33487

United States

Authorised Representative/ UK Responsible Person
Name: Delta Surgical Limited
Address:

Unit 10 Evolution Lymedale Business Park

Newcastle under Lyme

Staffordshire ST5 9QF

United Kingdom

Code/Term Type

Neurosurgical retraction cannula stabilization tool Neurosurgical retraction cannula stabilization tool Class III

Neurosurgical retraction cannula Neurosurgical retraction cannula Class III

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
Neurosurgical retraction cannula stabilization tool	Neurosurgical retraction cannula stabilization tool	Class III
Neurosurgical retraction cannula	Neurosurgical retraction cannula	Class III