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 209884. The device is manufactured by Medline International France SAS from France, classified as General Medical Device.

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MHRA Registered

General Medical Device

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Eyelid speculum, single-use

MHRA Device ID: 209884

Device Type

General Medical Device

Type

Class I

Status

DREGIY

Date Registered

Jan 31, 2025

Manufacturer Information

Name

Medline International France SAS

Address

5 Rue Charles Lindbergh

Chateaubriant, France

DJ Fang

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

Device Type

Type

Status

Date Registered

Name

Address

DJ Fang

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