"Philips" electrocardiograph
Taiwan·Risk Class 2·Philips Medizin Systeme Böblingen GmbH;; Philips North America LLC·Registered Dec 09, 2024 – Dec 09, 2029Active- Analysis ID
- 111b9bc94a10a53b1e4e75415f34208a
- Customs Code
- DHA05603748402
- Manufacturer Country
- United States;;Germany
- 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.2340 Telecardiogram
- Import Information
- import
- Registration Date
- Dec 09, 2024
- Expiry Date
- Dec 09, 2029
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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 111b9bc94a10a53b1e4e75415f34208a and manufactured by Philips Medizin Systeme Böblingen GmbH;; Philips North America LLC. 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 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.