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 - Circius Pharma AB

Address:

Södra Långebergsgatan 34-36

Göteborg

Askim 436 32

Sweden

Authorised Representative/ UK Responsible Person
Name: Kestrel Medical Ltd.
Address:

7 Moor Road

Broadstone

Dorset BH18 8AZ

United Kingdom

Code/Term Type

Middle ear decompressor positive pressure Middle ear decompressor positive pressure Class I

Drying otic solution Drying otic solution 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
Middle ear decompressor positive pressure	Middle ear decompressor positive pressure	Class I
Drying otic solution	Drying otic solution	Class I