Taiwan FDA registration 0d6cbd426ed274dfb0704c4efb8e2e5e
"Stephen" phosphorus reagent
TW: 「斯德必優」磷試劑
Taiwan·Risk Class 1·STANBIO LABORATORY·Registered May 23, 2006 – May 23, 2011CancelledRegistration details
- Analysis ID
- 0d6cbd426ed274dfb0704c4efb8e2e5e
- Customs Code
- DHA04400455506
Company information
- Manufacturer
- STANBIO LABORATORY
- Manufacturer Country
- United States
- Authorized Representative
- LINKSEAS TRADING CO., LTD.
Product details
- Intended Use
- Direct quantitative UV determination of inorganic phosphorus in human serum and urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1580 Phosphoric acid (inorganic) test system
- Import Information
- import
Dates and status
- Registration Date
- May 23, 2006
- Expiry Date
- May 23, 2011
- Cancellation Date
- Nov 30, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Stephen" phosphorus reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0d6cbd426ed274dfb0704c4efb8e2e5e and manufactured by STANBIO LABORATORY. The authorized representative in Taiwan is LINKSEAS TRADING CO., LTD..
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