"Philips" Central Monitoring Station
Taiwan·Risk Class 2·PHILIPS MEDICAL SYSTEMS·Registered Jun 13, 2005 – Jun 13, 2020Cancelled- Analysis ID
- b3414cbd93c2df49895e50a5b9ab162e
- Customs Code
- DHA00601139000
- Manufacturer
- PHILIPS MEDICAL SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1025 Arrhythmia Detectors and Alerts
- Import Information
- import
- Registration Date
- Jun 13, 2005
- Expiry Date
- Jun 13, 2020
- 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" Central Monitoring Station in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b3414cbd93c2df49895e50a5b9ab162e 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 Böblingen GmbH;; Philips North America LLC, 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.