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 - Kessel medintim GmbH

Address:

Kelsterbacher Strasse 28

Nordenstrasse 82

Morfelden-Walldorf

64546

Germany

Authorised Representative/ UK Responsible Person
Name: Psephos Limited
Address:

Sussex Innovation Centre Science Park Square

Falmer

Brighton

East Sussex BN1 9SB

England United Kingdom

Code/Term Type

Diaphragm pessary Diaphragm pessary Class IIb

Vaginal dilator Vaginal dilator Class I

Vaginal lubricant Vaginal lubricant Class I

Tourniquet cuff reusable Tourniquet cuff reusable Class I

Penile vacuum device Penile vacuum device Class I

Incontinence penis clamp reusable Incontinence penis clamp reusable Class I

Incontinence penis clamp reusable Incontinence penis clamp reusable Class IIa

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
Diaphragm pessary	Diaphragm pessary	Class IIb
Vaginal dilator	Vaginal dilator	Class I
Vaginal lubricant	Vaginal lubricant	Class I
Tourniquet cuff reusable	Tourniquet cuff reusable	Class I
Penile vacuum device	Penile vacuum device	Class I
Incontinence penis clamp reusable	Incontinence penis clamp reusable	Class I
Incontinence penis clamp reusable	Incontinence penis clamp reusable	Class IIa