"Philips" cardiac shock resuscitator
Taiwan·Risk Class 2·PHILIPS MEDICAL SYSTEMS·Registered Apr 16, 1997 – Feb 09, 2019Cancelled- Analysis ID
- 473d5b8f8ee9b0196a58ca671bbb9c51
- Customs Code
- DHA00600823004
- Manufacturer
- PHILIPS MEDICAL SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- Intended Use
- ．
- Product Type (Level 1)
- 0600 Intensive Care Unit and Cardiac Intensive Care Unit Equipment
- Import Information
- import
- Registration Date
- Apr 16, 1997
- Expiry Date
- Feb 09, 2019
- 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" cardiac shock resuscitator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 473d5b8f8ee9b0196a58ca671bbb9c51 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 Goldway (Shenzhen) Industrial Inc., and 1 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.