Endoscopic insufflation tubing set, single-use - UK MHRA Medical Device Registration

Endoscopic insufflation tubing set, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 169702. The device is manufactured by Covidien llc from United States, classified as System or Procedure Pack. The authorized representative in the UK is Medtronic Limited.

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Endoscopic insufflation tubing set, single-use

MHRA Device ID: 169702•Ref: 169702

Device Type

System or Procedure Pack

Devices

Endoscopic insufflation tubing set, single-use

Type

System or Procedure Pack

Date Registered

Nov 26, 2024

Last Updated

Dec 28, 2023

Manufacturer Information

Name

Covidien llc

Address

15 Hampshire Street

Mansfield, MA, United States

Created Date

Mar 26, 2021

Authorized Representative

Name

Medtronic Limited

Relationship Type

UK Responsible Person

Address

Building 9 Croxley Park

Watford, Herts, England, United Kingdom

Postcode: WD18 8WW

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Endoscopic insufflation tubing set, single-use - 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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