Eyelid speculum, single-use - UK MHRA Medical Device Registration

Eyelid speculum, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 127632. The device is manufactured by Sterisets Manufacturing S.A. from Portugal, classified as General Medical Device. The authorized representative in the UK is Qserve Group 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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Eyelid speculum, single-use

MHRA Device ID: 127632•Ref: 127632

Device Type

General Medical Device

Devices

Eyelid speculum, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

Sterisets Manufacturing S.A.

Address

Zona Industrial 1 - Lote 11 a 14

Penafiel, Guilhufe, Portugal

Created Date

Sep 24, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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Eyelid speculum, single-use - UK MHRA Medical Device Registration

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Devices

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Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

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DJ Fang

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