Taiwan FDA registration a2feedb4eecc77cbdae2182de93c7f21
“MEDIANA” Automated External Defibrillator
TW: “玫迪納”自動體外心臟除顫器
Taiwan·Risk Class 3·MD·MEDIANA CO., LTD.·Registered Oct 28, 2021 – Oct 28, 2026ActiveRegistration details
- Analysis ID
- a2feedb4eecc77cbdae2182de93c7f21
- License Form
- Ministry of Health Medical Device Import No. 035013
- Customs Code
- DHA05603501305
Company information
- Manufacturer
- MEDIANA CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- DERLIN BIOMEDICAL 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 28, 2021
- Expiry Date
- Oct 28, 2026
About this record
Access comprehensive regulatory information for “MEDIANA” Automated External Defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a2feedb4eecc77cbdae2182de93c7f21 and manufactured by MEDIANA CO., LTD.. The authorized representative in Taiwan is DERLIN BIOMEDICAL CO.,LTD..
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