Taiwan FDA registration cb64fe9f91a05aee5b0f40cef87ed87c
"Philips" automatic extracorporeal cardiac defibrous fibrillator
TW: "飛利浦"自動體外心臟去纖維顫動器
Taiwan·Risk Class 3·PHILIPS MEDICAL SYSTEMS·Registered Nov 13, 2012 – Feb 09, 2019CancelledRegistration details
- Analysis ID
- cb64fe9f91a05aee5b0f40cef87ed87c
- Customs Code
- DHA00600904807
Company information
- Manufacturer
- PHILIPS MEDICAL SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
Product details
- Product Type (Level 1)
- 0699 Other Intensive Care Unit & Cardiac Care Unit Equipment
- Import Information
- import
Dates and status
- Registration Date
- Nov 13, 2012
- Expiry Date
- Feb 09, 2019
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Philips" automatic extracorporeal cardiac defibrous fibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number cb64fe9f91a05aee5b0f40cef87ed87c and manufactured by PHILIPS MEDICAL SYSTEMS. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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