Taiwan FDA registration 8438adb1c8c785a2a407f06798fb311c
Juxi respirator tubing (unsterilized)
TW: “聚希”呼吸器管路（未滅菌）
Taiwan·Risk Class 1·GCMEDICA·Registered Jun 04, 2012 – Jun 04, 2017CancelledRegistration details
- Analysis ID
- 8438adb1c8c785a2a407f06798fb311c
- Customs Code
- DHA04600165307
Company information
- Manufacturer
- GCMEDICA
- Manufacturer Country
- China
- Authorized Representative
- BENQ MEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of the "Respirator Tubing (D.5975)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5975 Respirator Tubing
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jun 04, 2012
- Expiry Date
- Jun 04, 2017
- Cancellation Date
- Feb 25, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Juxi respirator tubing (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8438adb1c8c785a2a407f06798fb311c and manufactured by GCMEDICA. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.
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