Taiwan FDA registration a1331a0a204bd5522fc05e54e5a4cd7c
"Schiller" DEFIGARD Defibrillator and Monitor
TW: "席勒" 蒂芙格去顫監視器
Taiwan·Risk Class 3·MD·SCHILLER MEDICAL·Registered May 28, 2022 – May 28, 2027ActiveRegistration details
- Analysis ID
- a1331a0a204bd5522fc05e54e5a4cd7c
- License Form
- Ministry of Health Medical Device Import No. 035442
- Customs Code
- DHA05603544202
Company information
- Manufacturer
- SCHILLER MEDICAL
- Manufacturer Country
- France
- Authorized Representative
- FUTUREMED TECHNOLOGY CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E5310 Automated External Defibrillator System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 28, 2022
- Expiry Date
- May 28, 2027
About this record
Access comprehensive regulatory information for "Schiller" DEFIGARD Defibrillator and Monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a1331a0a204bd5522fc05e54e5a4cd7c and manufactured by SCHILLER MEDICAL. The authorized representative in Taiwan is FUTUREMED TECHNOLOGY CORPORATION.
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