Taiwan FDA registration 7e2c3dd68264eec1f0603cfb9f075304
“Physio-Control” LIFEPAK 20e Defibrillator/Monitor and accessories
TW: “菲康”來沛去顫器/監視器及附件
Taiwan·Risk Class 3·MD·PHYSIO-CONTROL, INC.·Registered Sep 13, 2016 – Sep 13, 2026ActiveRegistration details
- Analysis ID
- 7e2c3dd68264eec1f0603cfb9f075304
- License Form
- Ministry of Health Medical Device Import No. 028785
- Customs Code
- DHA05602878502
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 devices
- Product Type (Level 2)
- E5310 Automated External Defibrillator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 13, 2016
- Expiry Date
- Sep 13, 2026
About this record
Access comprehensive regulatory information for “Physio-Control” LIFEPAK 20e Defibrillator/Monitor 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 7e2c3dd68264eec1f0603cfb9f075304 and manufactured by PHYSIO-CONTROL, INC.. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices