"Fuqiang" wound drainage system
- Analysis ID
- 04112754fab7f6d7b5826db3bb365ab1
- Manufacturer
- FORTUNE MEDICAL INSTRUMENT CORP.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- FORTUNE MEDICAL INSTRUMENT CORP.
- Intended Use
- Limited to the first level of identification scope of "non-powered, single-patient, portable suction device (I.4680)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4680 Non-motive, single patient-use, carry-on suctioning device
- Import Information
- 國產;; QMS/QSD
- Registration Date
- Dec 29, 2006
- Expiry Date
- Dec 29, 2011
- Cancellation Date
- Feb 15, 2007
- Status
- Logged out
- Reason
- 自請註銷
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Access comprehensive regulatory information for "Fuqiang" wound drainage system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 04112754fab7f6d7b5826db3bb365ab1 and manufactured by FORTUNE MEDICAL INSTRUMENT CORP.. The authorized representative in Taiwan is FORTUNE MEDICAL INSTRUMENT CORP..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FORTUNE MEDICAL INSTRUMENT CORP., 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.