Surgical air pipeline regulator - UK MHRA Medical Device Registration
Surgical air pipeline regulator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 114988. 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.
Device Type
General Medical Device
Devices
Surgical air pipeline regulator
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Sep 5, 2024
Relationship Type
Address
Brookdale Road Chapeltown
Sheffield, South Yorkshire, United Kingdom
Postcode: S35 2PW
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