Taiwan FDA registration 15b2d600cdf83b216926cb5cae7942d1
Roche Kebas Blood Sugar Machine
TW: 羅氏可霸斯血糖機
Taiwan·Risk Class 2·ROCHE DIAGNOSTICS GMBH·Registered Sep 19, 2023 – Sep 19, 2028ActiveRegistration details
- Analysis ID
- 15b2d600cdf83b216926cb5cae7942d1
- Customs Code
- DHA05603622104
Company information
- Manufacturer
- ROCHE DIAGNOSTICS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- ROCHE DIAGNOSTICS LTD.
Product details
- Intended Use
- This product is an in vitro diagnostic instrument that can be used in conjunction with Cobas GLU test strips to quantitatively measure glucose in whole blood.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1345 Glucose Test System
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Sep 19, 2023
- Expiry Date
- Sep 19, 2028
About this record
Access comprehensive regulatory information for Roche Kebas Blood Sugar Machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 15b2d600cdf83b216926cb5cae7942d1 and manufactured by ROCHE DIAGNOSTICS GMBH. The authorized representative in Taiwan is ROCHE DIAGNOSTICS LTD..
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