"Philips" cardiac shock resuscitator
Taiwan·Risk Class 3·Philips Goldway (Shenzhen) Industrial Inc.·Registered Sep 09, 2019 – Sep 09, 2029Active- Analysis ID
- 8ddb2782fe384b3c9cffa32f0843dee6
- Customs Code
- DHA09200106605
- 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.5310 自動體外去顫器系統
- Import Information
- Input;; Chinese goods
- Registration Date
- Sep 09, 2019
- Expiry Date
- Sep 09, 2029
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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 3 medical device is registered under number 8ddb2782fe384b3c9cffa32f0843dee6 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, 1 companies making similar products including PHILIPS MEDICAL SYSTEMS, 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.