Laryngostroboscope - UK MHRA Medical Device Registration

Laryngostroboscope is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 125931. The device is manufactured by PENTAX of the Americas, Inc. from United States, 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.

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Laryngostroboscope

MHRA Device ID: 125931•Ref: 125931

Device Type

General Medical Device

Devices

Laryngostroboscope

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 22, 2024

Manufacturer Information

Name

PENTAX of the Americas, Inc.

Address

3 Paragon Drive

Montvale, United States

Created Date

Dec 2, 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

DJ Fang

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Other Products from PENTAX of the Americas, Inc. (4)

Other Products from Same Authorized Representative (10)

Laryngostroboscope - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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