"Philips" patient monitor
- Analysis ID
- f30c5d327e3e6b18a118895789df59e1
- Customs Code
- DHA00600800306
- Manufacturer
- PHILIPS MEDIZINSYSTEME BUBBLE GMBH;; 台灣飛利浦股份有限公司
- Manufacturer Country
- Taiwan, Province of China;;Germany
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- Intended Use
- Vacuum.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1025 Arrhythmia Detectors and Alerts
- Import Information
- import
- Registration Date
- Nov 26, 2009
- Expiry Date
- Feb 09, 2029
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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 f30c5d327e3e6b18a118895789df59e1 and manufactured by PHILIPS MEDIZINSYSTEME BUBBLE GMBH;; 台灣飛利浦股份有限公司. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including PHILIPS MEDIZINSYSTEME BÖBLINGEN GMBH, PHILIPS MEDICAL SYSTEMS, and 5 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.