Taiwan FDA registration 1980ff1c45795a0d2b39832992c6547e
“joimax” Shrill System
TW: “傑醫”希爾刨削系統
Taiwan·Risk Class 2·MD·JOIMAX GMBH·Registered Apr 15, 2019 – Apr 15, 2024ExpiredRegistration details
- Analysis ID
- 1980ff1c45795a0d2b39832992c6547e
- License Form
- Ministry of Health Medical Device Import No. 032508
- Customs Code
- DHA05603250804
Company information
- Manufacturer
- JOIMAX GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- K&C MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N1100 Arthroscopy
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 15, 2019
- Expiry Date
- Apr 15, 2024
About this record
Access comprehensive regulatory information for “joimax” Shrill System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1980ff1c45795a0d2b39832992c6547e and manufactured by JOIMAX GMBH. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices