Taiwan FDA registration 0c007660430fa339bfe57a456ea17074
"General medical" respirator tubing (unsterilized)
TW: “普醫”呼吸器管路 (未滅菌)
Taiwan·Risk Class 1·PROACT MEDICAL LTD.·Registered Oct 21, 2010 – Oct 21, 2015CancelledRegistration details
- Analysis ID
- 0c007660430fa339bfe57a456ea17074
- Customs Code
- DHA04400939101
Company information
- Manufacturer
- PROACT MEDICAL LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- PHOENIX INSTRUMENT BUSINESS CO., LTD.
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
- import
Dates and status
- Registration Date
- Oct 21, 2010
- Expiry Date
- Oct 21, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "General medical" 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 0c007660430fa339bfe57a456ea17074 and manufactured by PROACT MEDICAL LTD.. The authorized representative in Taiwan is PHOENIX INSTRUMENT BUSINESS CO., LTD..
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