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Ophthalmic fibreoptic light instrument, single-use - UK MHRA Medical Device Registration

Ophthalmic fibreoptic light instrument, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 106857. The device is manufactured by Katalyst Surgical LLC from United States, classified as General Medical Device. The authorized representative in the UK is M.I.S.S Ophthalmics 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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General Medical Device
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Ophthalmic fibreoptic light instrument, single-use
MHRA Device ID: 106857โ€ขRef: 106857

Device Type

General Medical Device

Devices

Ophthalmic fibreoptic light instrument, single-use

Type

Class IIa

Date Registered

Oct 5, 2021

Last Updated

Dec 22, 2022

Manufacturer Information

Address

754 Goddard Ave

Chesterfield, United States

Created Date

Oct 5, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

3 Ryder Court Saxon Way East Oakley Hay

Corby, Northamptonshire, England, United Kingdom

Postcode: NN18 9NX

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