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 - Pos-T-Vac LLC

Address:

2111 W. Wyatt Earp Blvd

Dodge City Kansas

67801

United States

Authorised Representative/ UK Responsible Person
Name: Wellkang Ltd
Address:

16 Castle St.

Dover

Kent CT16 1PW

England United Kingdom

Code/Term Type

Penile vacuum device Penile vacuum device Class I

Penile ring Penile ring Class I

Cartridge-accepting autoinjector mechanical Cartridge-accepting autoinjector mechanical Class I

Incontinence penis clamp reusable Incontinence penis clamp reusable 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
Penile vacuum device	Penile vacuum device	Class I
Penile ring	Penile ring	Class I
Cartridge-accepting autoinjector mechanical	Cartridge-accepting autoinjector mechanical	Class I
Incontinence penis clamp reusable	Incontinence penis clamp reusable	Class I