Taiwan FDA registration 33c233e18fd0c76c234c35fa4947cbf7
"Bode" manual arthroscopic equipment (sterile/unsterile)
TW: "鉑德" 手動式關節鏡器材(滅菌/未滅菌)
Taiwan·Risk Class 1·PolyDiagnost GmbH·Registered Aug 07, 2020 – Aug 07, 2025ExpiredRegistration details
- Analysis ID
- 33c233e18fd0c76c234c35fa4947cbf7
- Customs Code
- DHA09402184100
Company information
- Manufacturer
- PolyDiagnost GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- CHAWEI CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the classification and grading management method for medical equipment "Arthroscopy (N.1100)".
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.1100 Closing Lenses
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Aug 07, 2020
- Expiry Date
- Aug 07, 2025
About this record
Access comprehensive regulatory information for "Bode" manual arthroscopic equipment (sterile/unsterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 33c233e18fd0c76c234c35fa4947cbf7 and manufactured by PolyDiagnost GmbH. The authorized representative in Taiwan is CHAWEI 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