Flexible video duodenoscope, reusable - UK MHRA Medical Device Registration
Flexible video duodenoscope, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 166461. The device is manufactured by Hoya Corporation from Japan, classified as General Medical Device. The authorized representative in the UK is Pentax UK Ltd.
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Device Type
General Medical Device
Devices
Flexible video duodenoscope, reusable
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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