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Gonioscope - UK MHRA Medical Device Registration

Gonioscope is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 133007. The device is manufactured by Ocular Instruments, Inc from United States, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (UK) Limited .

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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General Medical Device
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Gonioscope
MHRA Device ID: 133007โ€ขRef: 133007

Device Type

General Medical Device

Devices

Gonioscope

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Apr 17, 2024

Manufacturer Information

Address

2255 116th ave NE

Bellevue, United States

Created Date

Jan 19, 2022

Authorized Representative

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 โ€“ UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

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