Lacrimal procedural cannula - UK MHRA Medical Device Registration

Lacrimal procedural cannula is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 95919. 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.

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Lacrimal procedural cannula

MHRA Device ID: 95919•Ref: 95919

Device Type

General Medical Device

Devices

Lacrimal procedural cannula

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jan 29, 2024

Manufacturer Information

Name

OASIS Medical, Inc.

Address

510-528 S. Vermont Avenue

Glendora, United States

Created Date

Apr 27, 2021

Authorized Representative

Name

Donawa Lifescience Ltd

Relationship Type

UK Responsible Person

Address

Aviation Business Park Enterprise Close

Christchurch, England, United Kingdom

Postcode: BH23 6NX

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Other Products from OASIS Medical, Inc. (10)

Other Products from Same Authorized Representative (10)

Lacrimal procedural cannula - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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