"Philips" electrocardiograph
Taiwan·Risk Class 2·PHILIPS MEDICAL SYSTEMS·Registered Sep 23, 2005 – Sep 23, 2020Cancelled- Analysis ID
- 340a7ccc521613d8550a6788da449cae
- Customs Code
- DHA00601199505
- 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.2340 Telecardiogram
- Import Information
- import
- Registration Date
- Sep 23, 2005
- Expiry Date
- Sep 23, 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" electrocardiograph in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 340a7ccc521613d8550a6788da449cae 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 Medizin Systeme Böblingen GmbH;; Philips North America LLC, ;; Philips Goldway (Shenzhen) Industrial Inc., 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.