Patient-controlled analgesia electric infusion pump administration set - UK MHRA Medical Device Registration

Patient-controlled analgesia electric infusion pump administration set is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 164151. The device is manufactured by Sendal S.L. from Spain, 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 electric infusion pump administration set

MHRA Device ID: 164151•Ref: 164151

Device Type

General Medical Device

Devices

Patient-controlled analgesia electric infusion pump administration set

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Sep 25, 2024

Manufacturer Information

Name

Sendal S.L.

Address

Ctra. Nacional Madrid-Caceres s/n

Almaraz, Caceres, Spain

Created Date

Jun 3, 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 electric infusion pump administration set - UK MHRA Medical Device Registration

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