Filiform urethral bougie - UK MHRA Medical Device Registration
Filiform urethral bougie is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 212517. The device is manufactured by STEMA Medizintechnik GmbH from Germany, classified as General Medical Device.
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Device Type
General Medical Device
Type
Class I
Status
Date Registered
Mar 6, 2025
Address
take-off GewerbePark 74
Neuhausen ob Eck, Germany
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