Taiwan FDA registration 9017830467eca0b95dba5885c580494a

"Febim" non-aerated tourniquet (sterilized)

TW: "費比姆"非充氣式止血帶(滅菌)

Taiwan·Risk Class 1·VBM MEDIZINTECHNIK GMBH·Registered Jan 23, 2019 – Jan 23, 2029Active

Registration details

Analysis ID: 9017830467eca0b95dba5885c580494a
Customs Code: DHA09402005204

Company information

Manufacturer: VBM MEDIZINTECHNIK GMBH
Manufacturer Country: Germany
Authorized Representative: NSH MEDICAL CORP.

Product details

Intended Use: Limited to the first level identification range of the "non-inflatable tourniquet (I.5900)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.5900 非充氣式止血帶
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Jan 23, 2019
Expiry Date: Jan 23, 2029

About this record

Access comprehensive regulatory information for "Febim" non-aerated tourniquet (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9017830467eca0b95dba5885c580494a and manufactured by VBM MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is NSH MEDICAL CORP..

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