Taiwan FDA registration 1fbadc421d5fc237e54d385f90cd1c6a
"Oka Shin" respiratory pipeline (unsterilized)
TW: “岡新”呼吸器管路(未滅菌)
Registration details
- Analysis ID
- 1fbadc421d5fc237e54d385f90cd1c6a
Company information
- Manufacturer
- KUNG SHIN PLASTICS CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- KUNG SHIN PLASTICS 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
- Domestic
Dates and status
- Registration Date
- Aug 10, 2010
- Expiry Date
- Aug 10, 2015
- Cancellation Date
- Jun 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Oka Shin" respiratory pipeline (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1fbadc421d5fc237e54d385f90cd1c6a and manufactured by KUNG SHIN PLASTICS CO., LTD.. The authorized representative in Taiwan is KUNG SHIN PLASTICS CO., LTD..
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