Taiwan FDA registration 44283774967e210721c87a3044b7338f
"Sontec" Orthopedic manual surgical instrument (Non-Sterile)
TW: "索尼克" 手動式骨科手術器械 (未滅菌)
Taiwan·Risk Class 1·MD·SONTEC INSTRUMENTS INC.·Registered Dec 02, 2013 – Dec 02, 2018CancelledRegistration details
- Analysis ID
- 44283774967e210721c87a3044b7338f
- License Form
- Ministry of Health Medical Device Import No. 013649
- Customs Code
- DHA09401364909
Company information
- Manufacturer
- SONTEC INSTRUMENTS INC.
- Manufacturer Country
- United States
- Authorized Representative
- PRO-READY ENTERPRISE CO., LTD.
Product details
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N4540 Manual osteologic surgery instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 02, 2013
- Expiry Date
- Dec 02, 2018
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for "Sontec" Orthopedic manual surgical instrument (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 44283774967e210721c87a3044b7338f and manufactured by SONTEC INSTRUMENTS INC.. The authorized representative in Taiwan is PRO-READY ENTERPRISE CO., LTD..
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