Taiwan FDA registration 103c873de6d7ccaaf938d21d8f4afca3
“JOIMAX” Orthopedics manual surgical instrument (Non-Sterile)
TW: “脊美適”手動式骨科手術器械(未滅菌)
Taiwan·Risk Class 1·MD·JOIMAX GMBH·Registered Jan 10, 2020 – Jan 10, 2025ExpiredRegistration details
- Analysis ID
- 103c873de6d7ccaaf938d21d8f4afca3
- License Form
- Ministry of Health Medical Device Import No. 021177
- Customs Code
- DHA09402117703
Company information
- Manufacturer
- JOIMAX GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- K&C MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N4540 Manual osteologic surgery instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 10, 2020
- Expiry Date
- Jan 10, 2025
About this record
Access comprehensive regulatory information for “JOIMAX” Orthopedics manual surgical instrument (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 103c873de6d7ccaaf938d21d8f4afca3 and manufactured by JOIMAX GMBH. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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