Taiwan FDA registration 3f0a44e2d8207162db46dc6a0620d8b2
Shinohara creatinine standard
TW: 筱原肌酸酐標準液
Taiwan·Risk Class 2·SHINO-TEST CORPORATION, SAGAMIHARA PRODUCTION CENTER·Registered Jun 04, 2012 – Jun 04, 2027ActiveRegistration details
- Analysis ID
- 3f0a44e2d8207162db46dc6a0620d8b2
- Customs Code
- DHA00602364701
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- Quantitative detection of creatinine in human serum, plasma, or urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1225 肌氨酸酐試驗系統(Creatininetestsystem)
- Import Information
- import
Dates and status
- Registration Date
- Jun 04, 2012
- Expiry Date
- Jun 04, 2027
About this record
Access comprehensive regulatory information for Shinohara creatinine standard in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3f0a44e2d8207162db46dc6a0620d8b2 and manufactured by SHINO-TEST CORPORATION, SAGAMIHARA PRODUCTION CENTER. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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