Taiwan FDA registration 3696cda6f3c1e182573ab8a076619de4
Kiromi IR Correction Solution II
TW: 喜樂美IR校正液II
Taiwan·Risk Class 2·SYNERMED INTERNATIONAL INC.·Registered Jun 30, 2006 – Jun 30, 2011CancelledRegistration details
- Analysis ID
- 3696cda6f3c1e182573ab8a076619de4
- Customs Code
- DHA00601717701
Company information
- Manufacturer
- SYNERMED INTERNATIONAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- PUREBLOOD-TECH INTERNATIONAL CORP.
Product details
- Intended Use
- 用於校正Synermed IR200分析儀、Synermed IR500分析儀、Hitachi系列分析儀、AU5000分析儀、AM Diagnostics Excel分析儀以及Roche Mira分析儀.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- import
Dates and status
- Registration Date
- Jun 30, 2006
- Expiry Date
- Jun 30, 2011
- 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 IR Correction Solution II in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3696cda6f3c1e182573ab8a076619de4 and manufactured by SYNERMED INTERNATIONAL INC.. The authorized representative in Taiwan is PUREBLOOD-TECH INTERNATIONAL CORP..
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