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Electrooculograph electrode - UK MHRA Medical Device Registration

Electrooculograph electrode is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 121301. The device is manufactured by Bovie Medical Corporation 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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Electrooculograph electrode
MHRA Device ID: 121301โ€ขRef: 121301

Device Type

General Medical Device

Devices

Electrooculograph electrode

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 11, 2024

Manufacturer Information

Address

5115 Ulmerton Road

Clearwater, Florida, United States

Created Date

Sep 1, 2021

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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