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.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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.
Device Type
General Medical Device
Type
Class I
Status
Date Registered
Jan 31, 2025
Address
5 Rue Charles Lindbergh
Chateaubriant, France
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