“Philips” IntelliVue Patient Monitor
Taiwan·Risk Class 2·MD·For use only by the Parts System Denda;;For spare parts system only;;Philips Medizin Systeme Böblingen GmbH·Registered Oct 19, 2021 – Oct 19, 2026Active- Analysis ID
- d5bc5ce47ecf94dd650ff9188d0ae007
- License Form
- Ministry of Health Medical Device Import No. 034602
- Customs Code
- DHA05603460206
- Manufacturer
- For use only by the Parts System Denda;;For spare parts system only;;Philips Medizin Systeme Böblingen GmbH
- Manufacturer Country
- Costa Rica;;United States;;Germany
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1025 Arrhythmia detector and alert
- Import Information
- Imported from abroad
- Registration Date
- Oct 19, 2021
- Expiry Date
- Oct 19, 2026
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Access comprehensive regulatory information for “Philips” IntelliVue 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 d5bc5ce47ecf94dd650ff9188d0ae007 and manufactured by For use only by the Parts System Denda;;For spare parts system only;;Philips Medizin Systeme Böblingen 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 MEDIZINSYSTEME BÖBLINGEN GMBH, and 1 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.