Taiwan FDA registration 31582cdb6ed97be8ea75a5d947d122fd
"Sindis" manual instruments for general surgery (unsterilized)
TW: “信迪思”一般手術用手動式器械（未滅菌）
Taiwan·Risk Class 1·SYNTHES (USA)·Registered Jun 02, 2009 – Jun 02, 2024CancelledRegistration details
- Analysis ID
- 31582cdb6ed97be8ea75a5d947d122fd
- Customs Code
- DHA04400778206
Company information
- Manufacturer
- SYNTHES (USA)
- Manufacturer Country
- United States
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
Dates and status
- Registration Date
- Jun 02, 2009
- Expiry Date
- Jun 02, 2024
- Cancellation Date
- May 26, 2020
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Sindis" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 31582cdb6ed97be8ea75a5d947d122fd and manufactured by SYNTHES (USA). The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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