Taiwan FDA registration f32c49118033cea44e4412a51c2ebaee
"Schiller" Fred portable automatic external defibrillator
TW: “席勒”費萊德可攜式自動體外去顫器
Taiwan·Risk Class 3·SCHILLER AG·Registered Oct 28, 2011 – Oct 28, 2026ActiveRegistration details
- Analysis ID
- f32c49118033cea44e4412a51c2ebaee
- Customs Code
- DHA00602291100
Company information
- Manufacturer
- SCHILLER AG
- Manufacturer Country
- Switzerland
- 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
- Oct 28, 2011
- Expiry Date
- Oct 28, 2026
About this record
Access comprehensive regulatory information for "Schiller" Fred portable 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 f32c49118033cea44e4412a51c2ebaee and manufactured by SCHILLER AG. The authorized representative in Taiwan is HI-CLEARANCE INC..
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