"Philips" delivery room information management system
Taiwan·Risk Class 2·PHILIPS MEDICAL SYSTEMS·Registered Oct 25, 2006 – Oct 25, 2016Cancelled- Analysis ID
- db90e6d72bd7b7bd1fda0dcd53e27c44
- Customs Code
- DHA00601738304
- 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)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.2740 Pre- and post-production monitoring systems and accessories
- Import Information
- import
- Registration Date
- Oct 25, 2006
- Expiry Date
- Oct 25, 2016
- Cancellation Date
- Apr 25, 2018
- Status
- Logged out
- Reason
- 自行鍵入
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Access comprehensive regulatory information for "Philips" delivery room information management system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number db90e6d72bd7b7bd1fda0dcd53e27c44 and manufactured by PHILIPS MEDICAL SYSTEMS. 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 MEDICAL SYSTEMS, 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.