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 - G. Pohl-Boskamp GmbH & Co. KG

Address:

Kieler Strasse 11 Hohenlockstedt

Schleswig-Holstein

25551

Germany

Authorised Representative/ UK Responsible Person
Name: Purple Orchid Health limited
Address:

Albany House 14 Shute End

Wokingham

RB40 1BJ

England United Kingdom

Code/Term Type

Bladder instillation barrier Bladder instillation barrier Class III

Keratolytic solution Keratolytic solution Class IIa

Oropharyngeal mucosa protection material Oropharyngeal mucosa protection material 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
Bladder instillation barrier	Bladder instillation barrier	Class III
Keratolytic solution	Keratolytic solution	Class IIa
Oropharyngeal mucosa protection material	Oropharyngeal mucosa protection material	Class IIa