"Philips" patient monitor
Taiwan·Risk Class 2·Philips Goldway (Shenzhen) Industrial Inc.·Registered Nov 09, 2021 – Nov 09, 2026Active- Analysis ID
- d3be6f859582a02e508310b4f66c80cb
- Customs Code
- DHA09200126804
- Manufacturer
- Philips Goldway (Shenzhen) Industrial Inc.
- Manufacturer Country
- China
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.2300 Cardiac monitor (including cardiac data and heart rate monitor)
- Import Information
- Input;; Chinese goods
- Registration Date
- Nov 09, 2021
- Expiry Date
- Nov 09, 2026
Top companies providing products similar to ""Philips" patient monitor"
Recently registered similar products
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 d3be6f859582a02e508310b4f66c80cb and manufactured by Philips Goldway (Shenzhen) Industrial Inc.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 5 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.