Taiwan FDA registration 177a5d23535ca9e8208322fc42a3286c
“Philips” HeartStart MRx Defibrillator /Monitor
TW: “飛利浦” 心臟電擊復甦器
Taiwan·Risk Class 3·MD·PHILIPS MEDICAL SYSTEMS·Registered Jun 02, 2017 – Jun 02, 2022ExpiredRegistration details
- Analysis ID
- 177a5d23535ca9e8208322fc42a3286c
- License Form
- Ministry of Health Medical Device Import No. 029780
- Customs Code
- DHA05602978000
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 devices
- Product Type (Level 2)
- E5310 Automated External Defibrillator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 02, 2017
- Expiry Date
- Jun 02, 2022
About this record
Access comprehensive regulatory information for “Philips” HeartStart MRx Defibrillator /Monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 177a5d23535ca9e8208322fc42a3286c and manufactured by PHILIPS MEDICAL SYSTEMS. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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