Taiwan FDA registration 37ba2dddd1d2ba74f1997ca5b3248148
"Clariance" Orthopedic manual surgical instrument (Non-Sterile)
TW: "克萊兒" 手動式骨科手術器械 (未滅菌)
Taiwan·Risk Class 1·MD·CLARIANCE·Registered Dec 29, 2014 – Dec 29, 2019CancelledRegistration details
- Analysis ID
- 37ba2dddd1d2ba74f1997ca5b3248148
- License Form
- Ministry of Health Medical Device Import No. 014802
- Customs Code
- DHA09401480209
Company information
- Manufacturer
- CLARIANCE
- Manufacturer Country
- France
- Authorized Representative
- LI MIN BIOTECH 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 29, 2014
- Expiry Date
- Dec 29, 2019
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Clariance" 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 37ba2dddd1d2ba74f1997ca5b3248148 and manufactured by CLARIANCE. The authorized representative in Taiwan is LI MIN BIOTECH CO., LTD..
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