Endaural wax extraction curette - UK MHRA Medical Device Registration

Endaural wax extraction curette is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 132939. The device is manufactured by Bionix, 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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Endaural wax extraction curette

MHRA Device ID: 132939•Ref: 132939

Device Type

General Medical Device

Devices

Endaural wax extraction curette

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jan 23, 2024

Manufacturer Information

Name

Bionix, LLC

Address

1670 Indian Wood Circle

Maumee, Ohio, United States

Created Date

Jan 18, 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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Endaural wax extraction curette - UK MHRA Medical Device Registration

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Date Registered

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Name

Address

Created Date

Name

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Address

DJ Fang

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