Taiwan FDA registration 9c2df9e7793f1c3c5ccd10bf93651169
"Quin Tron" Breath Tracker SC and accessory (Non-Sterile)
TW: "昆特蘿"醣類代謝呼氣分析儀及其配件(未滅菌)
Taiwan·Risk Class 1·MD·QuinTron Instrument Company, Inc.·Registered Jun 22, 2018 – Jun 22, 2028ActiveRegistration details
- Analysis ID
- 9c2df9e7793f1c3c5ccd10bf93651169
- License Form
- Ministry of Health Medical Device Import No. 019221
- Customs Code
- DHA09401922101
Company information
- Manufacturer
- QuinTron Instrument Company, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- IN FUNG CO., LTD.
Product details
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Devices "A.1820)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1820
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 22, 2018
- Expiry Date
- Jun 22, 2028
About this record
Access comprehensive regulatory information for "Quin Tron" Breath Tracker SC and accessory (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 9c2df9e7793f1c3c5ccd10bf93651169 and manufactured by QuinTron Instrument Company, Inc.. The authorized representative in Taiwan is IN FUNG CO., LTD..
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