Oesophageal bougie, single-use - UK MHRA Medical Device Registration

Oesophageal bougie, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 122066. The device is manufactured by Coloplast AS from Denmark, classified as General Medical Device. The authorized representative in the UK is Coloplast 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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Oesophageal bougie, single-use

MHRA Device ID: 122066•Ref: 122066

Device Type

General Medical Device

Devices

Oesophageal bougie, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Mar 15, 2024

Manufacturer Information

Name

Coloplast AS

Address

Holtedam 1

Humlebaek, Denmark

Created Date

Apr 23, 2021

Authorized Representative

Name

Coloplast Ltd

Relationship Type

UK Responsible Person

Address

Nene Hall Peterborough Business Park

Peterborough, Cambridgeshire, England, United Kingdom

Postcode: PE2 6FX

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Other Products from Coloplast AS (10)

Other Products from Same Authorized Representative (10)

Oesophageal bougie, 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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