“Philips” Patient Monitor
Taiwan·Risk Class 2·MD·For spare parts system only;;PHILIPS MEDICAL SYSTEMS BOEBLINGEN GMBH·Registered Jul 04, 2014 – Jul 04, 2024Expired- Analysis ID
- 0cbb38e840bc744e2484b5b1aa420268
- License Form
- Ministry of Health Medical Device Import No. 026390
- Customs Code
- DHA05602639008
- Manufacturer Country
- United States;;Germany
- 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
- Jul 04, 2014
- Expiry Date
- Jul 04, 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 0cbb38e840bc744e2484b5b1aa420268 and manufactured by For spare parts system only;;PHILIPS MEDICAL SYSTEMS BOEBLINGEN GMBH. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH;;For use only by the Parts System Denda;;For spare parts system only, and 2 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.