“Philips” IntelliVue Information Center iX
Taiwan·Risk Class 2·MD·PHILIPS MEDICAL SYSTEMS·Registered Dec 24, 2013 – Dec 24, 2018Cancelled- Analysis ID
- c3d1188c0e30da33f7e7e892f58540a4
- License Form
- Ministry of Health Medical Device Import No. 025674
- Customs Code
- DHA05602567404
- Manufacturer
- PHILIPS MEDICAL SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1025 Arrhythmia detector and alert
- Import Information
- Imported from abroad
- Registration Date
- Dec 24, 2013
- Expiry Date
- Dec 24, 2018
- Cancellation Date
- Jul 15, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for “Philips” IntelliVue Information Center iX in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c3d1188c0e30da33f7e7e892f58540a4 and manufactured by PHILIPS MEDICAL SYSTEMS. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including PHILIPS MEDICAL SYSTEMS, PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH, 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.