“Philips” Patient Monitor
Taiwan·Risk Class 2·MD·PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH;;For use only by the Parts System Denda;;For spare parts system only·Registered May 06, 2019 – May 06, 2024Expired- Analysis ID
- 717cd2ea08aa74c79d600a4102708c47
- License Form
- Ministry of Health Medical Device Import No. 032595
- Customs Code
- DHA05603259502
- Manufacturer
- PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH;;For use only by the Parts System Denda;;For spare parts system only
- Manufacturer Country
- China;;Germany;;Switzerland;;United States;;Costa Rica;;Poland
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1025 Arrhythmia detector and alert
- Import Information
- Imported from abroad
- Registration Date
- May 06, 2019
- Expiry Date
- May 06, 2024
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Access comprehensive regulatory information for “Philips” Patient Monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 717cd2ea08aa74c79d600a4102708c47 and manufactured by PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH;;For use only by the Parts System Denda;;For spare parts system only. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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