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 170137. The device is manufactured by PSI/EYE-KO, Inc. dba Anodyne Surgical from United States, classified as General Medical Device. The authorized representative in the UK is Advena Ltd.

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Lacrimal procedural cannula

MHRA Device ID: 170137•Ref: 170137

Device Type

General Medical Device

Devices

Lacrimal procedural cannula

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Nov 22, 2024

Manufacturer Information

Name

PSI/EYE-KO, Inc. dba Anodyne Surgical

Address

804 Corporate Centre Drive

O'Fallon, Missouri, United States

Created Date

Jan 10, 2022

Authorized Representative

Name

Advena Ltd

Relationship Type

UK Responsible Person

Address

Pure Offices Plato Close

Warwick, England, United Kingdom

Postcode: CV34 6WE

DJ Fang

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Lacrimal procedural cannula - UK MHRA Medical Device Registration

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