Flexible ultrasound gastroduodenoscope - UK MHRA Medical Device Registration

Flexible ultrasound gastroduodenoscope is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 205383. 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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Flexible ultrasound gastroduodenoscope

MHRA Device ID: 205383•Ref: 205383

Device Type

General Medical Device

Devices

Flexible ultrasound gastroduodenoscope

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Nov 21, 2024

Manufacturer Information

Name

Hoya Corporation

Address

PENTAX Life Care Division 1-1-110, Tsutsujigaoka Akishima-shi

Tokyo, Japan

Created Date

Mar 15, 2021

Authorized Representative

Name

Pentax UK Ltd

Relationship Type

UK Responsible Person

Address

Unit D1 Heron Drive Langley

Slough, Berks, England, United Kingdom

Postcode: sl3 8pn

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Flexible ultrasound gastroduodenoscope - UK MHRA Medical Device Registration

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