Flexible fibreoptic bronchoscope - UK MHRA Medical Device Registration
Flexible fibreoptic bronchoscope is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 97500. The device is manufactured by Hoya Corporation from Japan, classified as General Medical Device. The authorized representative in the UK is Pentax 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.
Device Type
General Medical Device
Devices
Flexible fibreoptic bronchoscope
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Nov 21, 2024
Name
Hoya CorporationAddress
PENTAX Life Care Division 1-1-110, Tsutsujigaoka Akishima-shi
Tokyo, Japan
Created Date
Mar 15, 2021
Name
Pentax UK LtdRelationship Type
Address
Unit D1 Heron Drive Langley
Slough, Berks, England, United Kingdom
Postcode: sl3 8pn
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