Epidural/intrathecal anaesthesia set, non-medicated - UK MHRA Medical Device Registration

Epidural/intrathecal anaesthesia set, non-medicated is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 76211. The device is manufactured by Teleflex Medical from Ireland, classified as General Medical Device. The authorized representative in the UK is TFX Group Ltd.

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Epidural/intrathecal anaesthesia set, non-medicated

MHRA Device ID: 76211•Ref: 76211

Device Type

General Medical Device

Devices

Epidural/intrathecal anaesthesia set, non-medicated

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Apr 12, 2024

Manufacturer Information

Name

Teleflex Medical

Address

IDA Business and Technology Park Dublin Road

Athlone, Co. Westmeath, Ireland

Created Date

Apr 19, 2021

Authorized Representative

Name

TFX Group Ltd

Relationship Type

UK Responsible Person

Address

Grosvenor House Horseshoe Crescent

Old Town Beaconsfield, England, United Kingdom

Postcode: HP9 1LJ

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Other Products from Teleflex Medical (10)

Other Products from Same Authorized Representative (10)

Epidural/intrathecal anaesthesia set, non-medicated - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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