"Philips" electrocardiograph
Taiwan·Risk Class 2·;; Philips Goldway (Shenzhen) Industrial Inc.·Registered Aug 25, 2017 – Mar 09, 2026Expired- Analysis ID
- 2901cee77b6f1e2937b682643164a2d3
- Customs Code
- DHA09200086708
- Manufacturer
- ;; Philips Goldway (Shenzhen) Industrial Inc.
- Manufacturer Country
- ;;China
- 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.2340 Telecardiogram
- Import Information
- Input;; Chinese goods
- Registration Date
- Aug 25, 2017
- Expiry Date
- Mar 09, 2026
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Access comprehensive regulatory information for "Philips" electrocardiograph in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2901cee77b6f1e2937b682643164a2d3 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, 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.