Taiwan FDA registration 3bde45b888f1135a51a5eb6bbf7618a9
"Forcor" high-frequency electrocautery treatment system
TW: “福可爾”高頻電燒治療系統
Taiwan·Risk Class 2·F Care Systems NV·Registered May 11, 2018 – May 11, 2023ExpiredRegistration details
- Analysis ID
- 3bde45b888f1135a51a5eb6bbf7618a9
- Customs Code
- DHA05603097703
Company information
- Manufacturer
- F Care Systems NV
- Manufacturer Country
- Belgium
- Authorized Representative
- INTERLINK MEDICAL ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4400 Cutting and hemostasis electric knives and accessories thereof
- Import Information
- The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input
Dates and status
- Registration Date
- May 11, 2018
- Expiry Date
- May 11, 2023
About this record
Access comprehensive regulatory information for "Forcor" high-frequency electrocautery treatment system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3bde45b888f1135a51a5eb6bbf7618a9 and manufactured by F Care Systems NV. The authorized representative in Taiwan is INTERLINK MEDICAL ENTERPRISE CO., LTD..
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