Taiwan FDA registration 7232d15a10e6fcbda9c9b0e8ffe75191
“LIFE ARK” AUTOMATED EXTERNAL DEFIBRILLATOR AND ACCESSORIES
TW: “生命方舟”自動體外心臟電擊去顫器及附件
Taiwan·Risk Class 3·MD·DERMACARE BIOMED INC.·Registered Sep 12, 2017 – Sep 12, 2027ActiveRegistration details
- Analysis ID
- 7232d15a10e6fcbda9c9b0e8ffe75191
- License Form
- Ministry of Health Medical Device Manufacturing No. 005866
Company information
- Manufacturer
- DERMACARE BIOMED INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DERMACARE BIOMED INC.
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
- Produced in Taiwan, China
Dates and status
- Registration Date
- Sep 12, 2017
- Expiry Date
- Sep 12, 2027
About this record
Access comprehensive regulatory information for “LIFE ARK” AUTOMATED 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 7232d15a10e6fcbda9c9b0e8ffe75191 and manufactured by DERMACARE BIOMED INC.. The authorized representative in Taiwan is DERMACARE BIOMED INC..
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