Taiwan FDA registration b77820da3601d1d05c85a52b3e40cb53
"Leif" spine surgery manual instruments (unsterilized)
TW: “萊夫”脊椎手術手動器械 (未滅菌)
Taiwan·Risk Class 1·LIFE INSTRUMENTS CORPORATION·Registered May 16, 2007 – May 16, 2012CancelledRegistration details
- Analysis ID
- b77820da3601d1d05c85a52b3e40cb53
- Customs Code
- DHA04400585803
Company information
- Manufacturer
- LIFE INSTRUMENTS CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- U-CHANTER ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Neurosurgical Devices (K.4535)".
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.4535 非動力式神經外科用器械
- Import Information
- import
Dates and status
- Registration Date
- May 16, 2007
- Expiry Date
- May 16, 2012
- Cancellation Date
- Apr 16, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Leif" spine surgery manual instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b77820da3601d1d05c85a52b3e40cb53 and manufactured by LIFE INSTRUMENTS CORPORATION. The authorized representative in Taiwan is U-CHANTER ENTERPRISE CO., LTD..
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