Taiwan FDA registration e91d3a11ff78983504ea113943fa5a5a
"Schiller" Fred lightweight automatic external defibrillator
TW: “席勒”費萊德輕型自動體外去顫器
Taiwan·Risk Class 3·SCHILLER MEDICAL·Registered Dec 14, 2012 – Dec 14, 2027ActiveRegistration details
- Analysis ID
- e91d3a11ff78983504ea113943fa5a5a
- Customs Code
- DHA00602425907
Company information
- Manufacturer
- SCHILLER MEDICAL
- Manufacturer Country
- France
- Authorized Representative
- HI-CLEARANCE INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.5310 自動體外去顫器系統
- Import Information
- import
Dates and status
- Registration Date
- Dec 14, 2012
- Expiry Date
- Dec 14, 2027
About this record
Access comprehensive regulatory information for "Schiller" Fred lightweight automatic 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 e91d3a11ff78983504ea113943fa5a5a and manufactured by SCHILLER MEDICAL. The authorized representative in Taiwan is HI-CLEARANCE INC..
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