Taiwan FDA registration b22458cd90c41a5079dc3ea3ac219b72
"Ficon" Laipei automatic external defibrillator and accessories
TW: “菲康”來沛自動體外去顫器及附件
Taiwan·Risk Class 3·PHYSIO-CONTROL, INC.·Registered Nov 15, 2012 – Nov 15, 2027ActiveRegistration details
- Analysis ID
- b22458cd90c41a5079dc3ea3ac219b72
- Customs Code
- DHA00602416702
Company information
- Manufacturer
- PHYSIO-CONTROL, INC.
- Manufacturer Country
- United States
- Authorized Representative
- K&C MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.5310 自動體外去顫器系統
- Import Information
- import
Dates and status
- Registration Date
- Nov 15, 2012
- Expiry Date
- Nov 15, 2027
About this record
Access comprehensive regulatory information for "Ficon" Laipei automatic external defibrillator and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number b22458cd90c41a5079dc3ea3ac219b72 and manufactured by PHYSIO-CONTROL, INC.. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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