Taiwan FDA registration ce5aaf492b58a4a79a89def945c9b7c6
“Physio-control” LIFEPAK CR2 defibrillator
TW: “菲康” 自動體外除顫器
Registration details
- Analysis ID
- ce5aaf492b58a4a79a89def945c9b7c6
- License Form
- Ministry of Health Medical Device Import No. 034878
- Customs Code
- DHA05603487808
Company information
- Manufacturer
- PHYSIO-CONTROL, INC.
- Manufacturer Country
- United States
- Authorized Representative
- K&C MEDICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E5310 Automated External Defibrillator System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 18, 2021
- Expiry Date
- Oct 18, 2026
About this record
Access comprehensive regulatory information for “Physio-control” LIFEPAK CR2 defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number ce5aaf492b58a4a79a89def945c9b7c6 and manufactured by PHYSIO-CONTROL, INC.. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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