Taiwan FDA registration 595ae5d6f1d487afded97b4e2eb2faad
"Opiti" clinical sounder (unsterilized)
TW: “奧沛迪” 臨床用測深器(未滅菌)
Taiwan·Risk Class 1·OrthoPediatrics Corp.·Registered Sep 20, 2018 – Sep 20, 2023ExpiredRegistration details
- Analysis ID
- 595ae5d6f1d487afded97b4e2eb2faad
- Customs Code
- DHA09401962502
Company information
- Manufacturer
- OrthoPediatrics Corp.
- Manufacturer Country
- United States
- Authorized Representative
- A PLUS BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of clinical sounder (N.4300) of the medical equipment management measures.
- 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
- Sep 20, 2018
- Expiry Date
- Sep 20, 2023
About this record
Access comprehensive regulatory information for "Opiti" 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 595ae5d6f1d487afded97b4e2eb2faad and manufactured by OrthoPediatrics Corp.. The authorized representative in Taiwan is A PLUS BIOTECHNOLOGY 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