Taiwan FDA registration 82e19361cae1d3dc976fe4ac0123ff03
“Schiller” FRED PA-1 Automated External Defibrillator (AED)
TW: “席樂” 費萊德 皮耶萬 自動體外去顫器
Taiwan·Risk Class 3·MD·Schiller Medical·Registered Nov 20, 2017 – Nov 20, 2027ActiveRegistration details
- Analysis ID
- 82e19361cae1d3dc976fe4ac0123ff03
- License Form
- Ministry of Health Medical Device Import No. 030428
- Customs Code
- DHA05603042809
Company information
- Manufacturer
- Schiller Medical
- Manufacturer Country
- France
- Authorized Representative
- FUTUREMED TECHNOLOGY CORPORATION
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
- Nov 20, 2017
- Expiry Date
- Nov 20, 2027
About this record
Access comprehensive regulatory information for “Schiller” FRED PA-1 Automated External Defibrillator (AED) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 82e19361cae1d3dc976fe4ac0123ff03 and manufactured by Schiller Medical. The authorized representative in Taiwan is FUTUREMED TECHNOLOGY CORPORATION.
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