Taiwan FDA registration ab49cd8a1cf3c59096329f6c396dfd31
"Sindeli" Clinical Sounder (Unsterilized)
TW: "信德立" 臨床用測深計 (未滅菌)
Taiwan·Risk Class 1·Syntellix AG·Registered Jul 03, 2020 – Jul 03, 2025ExpiredRegistration details
- Analysis ID
- ab49cd8a1cf3c59096329f6c396dfd31
- Customs Code
- DHA09402169703
Company information
- Manufacturer
- Syntellix AG
- Manufacturer Country
- Germany
- Authorized Representative
- MEDLION BIOTECH CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the classification and grading management measures for medical equipment "Clinical Sothymetry (N.4300)".
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4300 臨床用測深計
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jul 03, 2020
- Expiry Date
- Jul 03, 2025
- Cancellation Date
- Nov 29, 2024
About this record
Access comprehensive regulatory information for "Sindeli" Clinical Sounder (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ab49cd8a1cf3c59096329f6c396dfd31 and manufactured by Syntellix AG. The authorized representative in Taiwan is MEDLION BIOTECH 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