Endoscope antifog solution - UK MHRA Medical Device Registration

Endoscope antifog solution is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 99683. The device is manufactured by Aesculap AG from Germany, classified as General Medical Device. The authorized representative in the UK is B. Braun Medical 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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Endoscope antifog solution

MHRA Device ID: 99683•Ref: 99683

Device Type

General Medical Device

Devices

Endoscope antifog solution

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Sep 5, 2024

Manufacturer Information

Name

Aesculap AG

Address

Am Aesculap Platz

Tuttlingen, Germany

Created Date

Mar 26, 2021

Authorized Representative

Name

B. Braun Medical Ltd

Relationship Type

UK Responsible Person

Address

Brookdale Road Chapeltown

Sheffield, South Yorkshire, United Kingdom

Postcode: S35 2PW

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Endoscope antifog solution - UK MHRA Medical Device Registration

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