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 158796. The device is manufactured by Adroit Surgical LLC from United States, classified as General Medical Device. The authorized representative in the UK is Obelis 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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Oesophageal bougie, single-use

MHRA Device ID: 158796•Ref: 158796

Device Type

General Medical Device

Devices

Oesophageal bougie, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jan 23, 2024

Manufacturer Information

Name

Adroit Surgical LLC

Address

10001 Broadway Extension Suite A

Oklahoma City, United States

Created Date

Oct 21, 2022

Authorized Representative

Name

Obelis UK Ltd

Relationship Type

UK Responsible Person

Address

Sandford Gate, East Point Business Park

Oxford , England, United Kingdom

Postcode: OX4 6LB

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Other Products from Adroit Surgical LLC (2)

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Type: General Medical Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

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

Device Type

Devices

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Date Registered

Last Updated

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Created Date

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Address

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