Taiwan FDA registration 6b48d09cd3d05809a8b2caae5d3dc295
Kiromi alkaline phosphatase reagent
TW: 喜樂美鹼性磷酸酶試劑
Taiwan·SYNERMED INTERNATIONAL INC.·Registered Oct 26, 2005 – Oct 26, 2010CancelledRegistration details
- Analysis ID
- 6b48d09cd3d05809a8b2caae5d3dc295
- Customs Code
- DHA00601325402
Company information
- Manufacturer
- SYNERMED INTERNATIONAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- PUREBLOOD-TECH INTERNATIONAL CORP.
Product details
- Intended Use
- Quantify the amount of frenetic phosphatase in human serum.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Import Information
- import
Dates and status
- Registration Date
- Oct 26, 2005
- Expiry Date
- Oct 26, 2010
- Cancellation Date
- Nov 26, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Kiromi alkaline phosphatase reagent in Taiwan's medical device market through Pure Global AI's free database. is registered under number 6b48d09cd3d05809a8b2caae5d3dc295 and manufactured by SYNERMED INTERNATIONAL INC.. The authorized representative in Taiwan is PUREBLOOD-TECH INTERNATIONAL CORP..
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