Patient-controlled analgesia infusion pump - UK MHRA Medical Device Registration

Patient-controlled analgesia infusion pump is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 69157. The device is manufactured by CareFusion 303, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Becton, Dickinson U.K. Limited.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Patient-controlled analgesia infusion pump

MHRA Device ID: 69157•Ref: 69157

Device Type

General Medical Device

Devices

Patient-controlled analgesia infusion pump

Type

Class IIb

Date Registered

Mar 11, 2021

Last Updated

Nov 14, 2023

Manufacturer Information

Name

CareFusion 303, Inc.

Address

10020 Pacific Mesa Boulevard

San Diego, California, United States

Created Date

Mar 11, 2021

Authorized Representative

Name

Becton, Dickinson U.K. Limited

Relationship Type

UK Responsible Person

Address

1030 Eskdale Road Winnersh Triangle, Wokingham

Winnersh, England, United Kingdom

Postcode: RG41 5TS

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Patient-controlled analgesia infusion pump - UK MHRA Medical Device Registration

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