Taiwan FDA registration 17df41129bd5c8babeed2099f8816dd0
"JOIMAX" Spinal Endoscopic Instruments (Non-Sterile)
TW: "脊美適" 脊椎內視鏡工具 (未滅菌)
Taiwan·Risk Class 1·MD·JOIMAX GMBH·Registered May 05, 2015 – May 05, 2025ExpiredRegistration details
- Analysis ID
- 17df41129bd5c8babeed2099f8816dd0
- License Form
- Ministry of Health Medical Device Import No. 015192
- Customs Code
- DHA09401519200
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 "Arthroscopy (N.1100)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N1100 Arthroscopy
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 05, 2015
- Expiry Date
- May 05, 2025
About this record
Access comprehensive regulatory information for "JOIMAX" Spinal Endoscopic Instruments (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 17df41129bd5c8babeed2099f8816dd0 and manufactured by JOIMAX GMBH. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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