Taiwan FDA registration 5b86506edd1d95f2c15eda7e6146ee7b
Kiromi uric acid reagent
TW: 喜樂美尿酸試劑
Taiwan·Risk Class 1·SYNERMED INTERNATIONAL INC.·Registered Jul 29, 2005 – Jul 29, 2010CancelledRegistration details
- Analysis ID
- 5b86506edd1d95f2c15eda7e6146ee7b
- Customs Code
- DHA04400028802
Company information
- Manufacturer
- SYNERMED INTERNATIONAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- PUREBLOOD-TECH INTERNATIONAL CORP.
Product details
- Intended Use
- It is used to measure the level of uric acid in human serum or blood.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Import Information
- import
Dates and status
- Registration Date
- Jul 29, 2005
- Expiry Date
- Jul 29, 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 uric acid reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5b86506edd1d95f2c15eda7e6146ee7b and manufactured by SYNERMED INTERNATIONAL INC.. The authorized representative in Taiwan is PUREBLOOD-TECH INTERNATIONAL CORP..
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