Taiwan FDA registration 9379fc1033c19ea31b383ea0bdda855c
"Radiel" clinical sample (unsterilized)
TW: "樂迪爾" 臨床用樣板 (未滅菌)
Taiwan·Risk Class 1·LDR MEDICAL·Registered Mar 23, 2015 – Mar 23, 2020CancelledRegistration details
- Analysis ID
- 9379fc1033c19ea31b383ea0bdda855c
- Customs Code
- DHA09401503000
Company information
- Manufacturer
- LDR MEDICAL
- Manufacturer Country
- France
- Authorized Representative
- HOLLING BIO-PHARMA. CORP.
Product details
- Intended Use
- Limited to the first level identification range of the "clinical use model (N.4800)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4800 Sample plate for clinical use
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Mar 23, 2015
- Expiry Date
- Mar 23, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Radiel" clinical sample (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9379fc1033c19ea31b383ea0bdda855c and manufactured by LDR MEDICAL. The authorized representative in Taiwan is HOLLING BIO-PHARMA. CORP..
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