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

Back to MHRA

Manufacturer's Devices - Dr. Jean Bausch GmbH & Co. KG

Address:

Oskar-Schindler-Strasse 4

Cologne

Northrhine-Westfalia (NW) 50769

Germany

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

Sandford Gate East Point Business Park

Oxford

OX4 6LB

England United Kingdom

Code/Term Type

Dental articulation paper Dental articulation paper Class I

Dental articulation paste/solution Dental articulation paste/solution Class I

Dental articulation paper forceps Dental articulation paper forceps Class I

Interproximal/occlusal dental gauge single-use Interproximal/occlusal dental gauge single-use 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
Dental articulation paper	Dental articulation paper	Class I
Dental articulation paste/solution	Dental articulation paste/solution	Class I
Dental articulation paper forceps	Dental articulation paper forceps	Class I
Interproximal/occlusal dental gauge single-use	Interproximal/occlusal dental gauge single-use	Class I