Taiwan FDA registration 53f151b75673c7c0e4efa55a35685ec8
"FZK" Mechanical wheelchair (Non-Sterile)
TW: "富士康" 機械式輪椅 (未滅菌)
Registration details
- Analysis ID
- 53f151b75673c7c0e4efa55a35685ec8
- License Form
- Ministry of Health Medical Device Import No. 016842
- Customs Code
- DHA09401684205
Company information
- Manufacturer
- A&I VIETNAM MEDICAL EQUIPMENT CO., LTD.
- Manufacturer Country
- Viet Nam
- Authorized Representative
- FUZIKON MEDICAL EQUIPMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Mechanical Wheelchair (O.3850)".
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3850 mechanical wheelchair
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 29, 2016
- Expiry Date
- Jul 29, 2021
About this record
Access comprehensive regulatory information for "FZK" Mechanical wheelchair (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 53f151b75673c7c0e4efa55a35685ec8 and manufactured by A&I VIETNAM MEDICAL EQUIPMENT CO., LTD.. The authorized representative in Taiwan is FUZIKON MEDICAL EQUIPMENT CO., LTD..
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