Taiwan FDA registration 2e301d782cc7248d24b6917a54b49de8
“Schiller” Defibrillators with monitoring functionality
TW: “席樂” 德培克 觸控式生理監視去顫器
Taiwan·Risk Class 3·MD·Schiller Medical·Registered Dec 07, 2017 – Dec 07, 2027ActiveRegistration details
- Analysis ID
- 2e301d782cc7248d24b6917a54b49de8
- License Form
- Ministry of Health Medical Device Import No. 030610
- Customs Code
- DHA05603061001
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
- Dec 07, 2017
- Expiry Date
- Dec 07, 2027
About this record
Access comprehensive regulatory information for “Schiller” Defibrillators with monitoring functionality in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2e301d782cc7248d24b6917a54b49de8 and manufactured by Schiller Medical. The authorized representative in Taiwan is FUTUREMED TECHNOLOGY CORPORATION.
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