Spectacle frame - UK MHRA Medical Device Registration

Spectacle frame is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 162034. The device is manufactured by EYEVAN Inc. from Japan, classified as General Medical Device. The authorized representative in the UK is AF PHARMA SERVICE UK 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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Spectacle frame

MHRA Device ID: 162034•Ref: 162034

Device Type

General Medical Device

Devices

Spectacle frame

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Nov 23, 2024

Manufacturer Information

Name

EYEVAN Inc.

Address

1-15-33 Minami-aoyama, Minaoto-ku

Tokyo, Japan

Created Date

Nov 29, 2022

Authorized Representative

Name

AF PHARMA SERVICE UK LTD

Relationship Type

UK Responsible Person

Address

Suite 140 Temple Chambers 3-7 Temple Avenue

London, England, United Kingdom

Postcode: EC4Y 0DA

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Spectacle frame - UK MHRA Medical Device Registration

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