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Ophthalmic sponge - UK MHRA Medical Device Registration

Ophthalmic sponge is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 95932. The device is manufactured by OASIS Medical, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Donawa Lifescience 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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Ophthalmic sponge
MHRA Device ID: 95932โ€ขRef: 95932

Device Type

General Medical Device

Devices

Ophthalmic sponge

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jan 29, 2024

Manufacturer Information

Address

510-528 S. Vermont Avenue

Glendora, United States

Created Date

Apr 27, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Aviation Business Park Enterprise Close

Christchurch, England, United Kingdom

Postcode: BH23 6NX

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