Bone file/rasp, manual, single-use - UK MHRA Medical Device Registration
Bone file/rasp, manual, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 207035. The device is manufactured by Neo Medical SA from Switzerland, classified as General Medical Device.
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Device Type
General Medical Device
Type
Class IIa
Status
Date Registered
Dec 17, 2024
Name
Neo Medical SAAddress
Route de Lausanne 157
Villette, Switzerland
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