Taiwan FDA registration e87b7e7c58dcb979042f24febdf25efb
"Philips" automatic external defibrillator
TW: “飛利浦”啟心自動體外去顫器
Taiwan·Risk Class 2·PHILIPS MEDICAL SYSTEMS·Registered Oct 03, 2011 – Oct 03, 2016CancelledRegistration details
- Analysis ID
- e87b7e7c58dcb979042f24febdf25efb
- Customs Code
- DHA00602283102
Company information
- Manufacturer
- PHILIPS MEDICAL SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
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 03, 2011
- Expiry Date
- Oct 03, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Philips" automatic external defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e87b7e7c58dcb979042f24febdf25efb and manufactured by PHILIPS MEDICAL SYSTEMS. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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