Intravenous line recessed-needle connector - UK MHRA Medical Device Registration

Intravenous line recessed-needle connector is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 97334. The device is manufactured by Invivo, a division of Philips Medical Systems from United States, classified as General Medical Device. The authorized representative in the UK is Philips Electronics UK Ltd.

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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Intravenous line recessed-needle connector

MHRA Device ID: 97334•Ref: 97334

Device Type

General Medical Device

Devices

Intravenous line recessed-needle connector

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jun 20, 2024

Manufacturer Information

Name

Invivo, a division of Philips Medical Systems

Address

12151 Research Parkway

Orlando, Florida, United States

Created Date

Aug 23, 2021

Authorized Representative

Name

Philips Electronics UK Ltd

Relationship Type

UK Responsible Person

Address

Ascent 1 Farnborough Aerospace Centre

Farnborough, Hampshire, England, United Kingdom

Postcode: GU14 6XW

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Intravenous line recessed-needle connector - UK MHRA Medical Device Registration

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