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 - Baxter Hechingen

Address:

Linsenaecker 1

Hechingen

72379

Germany

Authorised Representative/ UK Responsible Person
Name: Baxter Healthcare Ltd
Address:

Caxton Way

Thetford

Norfolk IP24 3SQ

England United Kingdom

Code/Term Type

Double-lumen haemodialysis catheter nonimplantable Double-lumen haemodialysis catheter nonimplantable Class III

Luer-formatted protective cap Luer-formatted protective cap Class IIa

Peripheral vascular guidewire manual Peripheral vascular guidewire manual Class IIa

Pressure-management bandage padded Pressure-management bandage padded Class IIa

Pressure-management bandage padded Pressure-management bandage padded 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
Double-lumen haemodialysis catheter nonimplantable	Double-lumen haemodialysis catheter nonimplantable	Class III
Luer-formatted protective cap	Luer-formatted protective cap	Class IIa
Peripheral vascular guidewire manual	Peripheral vascular guidewire manual	Class IIa
Pressure-management bandage padded	Pressure-management bandage padded	Class IIa
Pressure-management bandage padded	Pressure-management bandage padded	Class I