Taiwan FDA registration bc927bacbc305ea0e101f5c9d0667ad1
"Kindi" medical absorbent fiber (unsterilized)
TW: “金蒂”醫療用吸收纖維(未滅菌)
Taiwan·Risk Class 1·HENAN PIAOAN GROUP CO., LTD.·Registered Dec 18, 2008 – Dec 18, 2018CancelledRegistration details
- Analysis ID
- bc927bacbc305ea0e101f5c9d0667ad1
- Customs Code
- DHA04600060402
Company information
- Manufacturer
- HENAN PIAOAN GROUP CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- KING DAY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Medical Absorbent Fiber (J.5300)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5300 醫療用吸收纖維
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Dec 18, 2008
- Expiry Date
- Dec 18, 2018
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Kindi" medical absorbent fiber (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bc927bacbc305ea0e101f5c9d0667ad1 and manufactured by HENAN PIAOAN GROUP CO., LTD.. The authorized representative in Taiwan is KING DAY CO., LTD..
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