Taiwan FDA registration 6b431219c0b60c0314eedf2cb3070b4f
Manual orthopedic instruments "Ledel" (sterile/unsterile)
TW: "樂德爾"手動式骨科手術器械(滅菌/未滅菌)
Taiwan·Risk Class 1·LDR Medical·Registered Sep 24, 2014 – Sep 24, 2019CancelledRegistration details
- Analysis ID
- 6b431219c0b60c0314eedf2cb3070b4f
- Customs Code
- DHA09401452904
Company information
- Manufacturer
- LDR Medical
- Manufacturer Country
- France
- Authorized Representative
- ZIMMER BIOMET TAIWAN CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4540 手動式骨科手術器械
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Sep 24, 2014
- Expiry Date
- Sep 24, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Manual orthopedic instruments "Ledel" (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 6b431219c0b60c0314eedf2cb3070b4f and manufactured by LDR Medical. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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