Taiwan FDA registration 2a4dc6e0ff32abfbcbad557efacbc84e
"Arkra" urine analyzer (unsterilized)
TW: 〝愛科來〞尿液分析儀 (未滅菌)
Taiwan·Risk Class 1·ARKRAY FACTORY INC.·Registered Dec 24, 2010 – Dec 24, 2015CancelledRegistration details
- Analysis ID
- 2a4dc6e0ff32abfbcbad557efacbc84e
- Customs Code
- DHA04400974102
Company information
- Manufacturer
- ARKRAY FACTORY INC.
- Manufacturer Country
- Japan
- Authorized Representative
- SYNGEN BIOTECH CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Automatic Urinalysis System (A.2900)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2900 Automated urinalysis system
- Import Information
- import
Dates and status
- Registration Date
- Dec 24, 2010
- Expiry Date
- Dec 24, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Arkra" urine analyzer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2a4dc6e0ff32abfbcbad557efacbc84e and manufactured by ARKRAY FACTORY INC.. The authorized representative in Taiwan is SYNGEN BIOTECH CO., LTD..
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