Subcutaneous infusion/injection port needle - UK MHRA Medical Device Registration

Subcutaneous infusion/injection port needle is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 193048. The device is manufactured by PROMEPLA S.A.M. from Monaco, classified as General Medical Device. The authorized representative in the UK is International Associates Limited.

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Subcutaneous infusion/injection port needle

MHRA Device ID: 193048•Ref: 193048

Device Type

General Medical Device

Devices

Subcutaneous infusion/injection port needle

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Sep 25, 2024

Manufacturer Information

Name

PROMEPLA S.A.M.

Address

9 avenue Albert II

Monte Carlo, Monaco

Created Date

Dec 21, 2023

Authorized Representative

Name

International Associates Limited

Relationship Type

UK Responsible Person

Address

38 Queen Street

Glasgow, Scotland, United Kingdom

Postcode: G1 3DX

DJ Fang

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Subcutaneous infusion/injection port needle - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Address

Created Date

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Address

DJ Fang

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