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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 90384. The device is manufactured by Synergetics, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Bausch & Lomb U.K. 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: 90384โ€ขRef: 90384

Device Type

General Medical Device

Devices

Ophthalmic fibreoptic light instrument, single-use

Type

Class IIa

Date Registered

Apr 11, 2024

Last Updated

Dec 2, 2023

Manufacturer Information

Address

3845 Corporate Centre Drive

Oโ€™Fallon, Missouri, United States

Created Date

Jul 23, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

106-114 London Road

Kingston upon Thames, Surrey, England, United Kingdom

Postcode: KT2 6TN

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