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 - CareFusion 303 Inc.

Address:

10020 Pacific Mesa Boulevard

San Diego

California 92121

United States

Authorised Representative/ UK Responsible Person
Name: Becton Dickinson U.K. Limited
Address:

1030 Eskdale Road Winnersh Triangle Wokingham

Winnersh

RG41 5TS

England United Kingdom

Code/Term Type

Bedside infusion pump single-channel Bedside infusion pump single-channel Class IIb

Bedside syringe pump Bedside syringe pump Class IIb

Patient-controlled analgesia infusion pump Patient-controlled analgesia infusion pump Class IIb

Infusion pump medication-dosage application software Infusion pump medication-dosage application software Class IIb

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
Bedside infusion pump single-channel	Bedside infusion pump single-channel	Class IIb
Bedside syringe pump	Bedside syringe pump	Class IIb
Patient-controlled analgesia infusion pump	Patient-controlled analgesia infusion pump	Class IIb
Infusion pump medication-dosage application software	Infusion pump medication-dosage application software	Class IIb