Taiwan FDA registration 8ef940726a8f6d9152d530499b4189f6
Fukushima rapid reagent cartridge reader
TW: 福島快速試劑匣判讀機
Taiwan·Risk Class 1·VEDA LAB·Registered Mar 16, 2006 – Mar 16, 2016CancelledRegistration details
- Analysis ID
- 8ef940726a8f6d9152d530499b4189f6
- Customs Code
- DHA04400297008
Company information
- Manufacturer
- VEDA LAB
- Manufacturer Country
- France
- Authorized Representative
- Fukushima Medical Equipment Co., Ltd
Product details
- Intended Use
- Quantitative or semi-quantitative interpretation of test results with immunochromatography cartridges used in this system.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2400 Density Meter/Sweeper for Clinical Use (Separation, Reflection, Thin Layer or Radioactive Color Layer Analysis)
- Import Information
- import
Dates and status
- Registration Date
- Mar 16, 2006
- Expiry Date
- Mar 16, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Fukushima rapid reagent cartridge reader in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8ef940726a8f6d9152d530499b4189f6 and manufactured by VEDA LAB. The authorized representative in Taiwan is Fukushima Medical Equipment Co., Ltd.
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