"GE" water trap (Non-Sterile)
Taiwan·Risk Class 1·MD·GE Healthcare·Registered Apr 27, 2016 – Apr 27, 2026Expired- Analysis ID
- a427c6a5616d65a93aa9639b6b59e69b
- License Form
- Ministry of Health Medical Device Import No. 016462
- Customs Code
- DHA09401646208
- Manufacturer
- GE Healthcare
- Manufacturer Country
- Estonia
- Authorized Representative
- GE MEDICAL SYSTEMS TAIWAN, LTD.
- Intended Use
- Limited to the first level identification range of the "T-shaped drainage (water collector) (D.5995)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5995 T-drain (water collector)
- Import Information
- Imported from abroad
- Registration Date
- Apr 27, 2016
- Expiry Date
- Apr 27, 2026
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Access comprehensive regulatory information for "GE" water trap (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a427c6a5616d65a93aa9639b6b59e69b and manufactured by GE Healthcare. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GE HEALTHCARE, 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.