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 - Prytime Medical Devices Inc.

Address:

229 North Main Street

Boerne

Texas 18006

United States

Authorised Representative/ UK Responsible Person
Name: MPS Medical-Product-Service UK Ltd
Address:

Northgate House Northgate Street

Devizes

Wiltshire SN10 1JX

England United Kingdom

Code/Term Type

General surgical procedure kit non-medicated single-use General surgical procedure kit non-medicated single-use

Intravascular occluding balloon catheter image-guided Intravascular occluding balloon catheter image-guided 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
General surgical procedure kit non-medicated single-use	General surgical procedure kit non-medicated single-use
Intravascular occluding balloon catheter image-guided	Intravascular occluding balloon catheter image-guided	Class III