Taiwan FDA registration 380d4676061ac2efa96f7323fcce7e2e
"Arkola" serum urea nitrogen test strip
TW: "愛科來"血清尿素氮檢測試紙
Taiwan·Risk Class 2·ARKRAY Factory, Inc., Head office factory·Registered Dec 22, 2005 – Dec 22, 2025ExpiredRegistration details
- Analysis ID
- 380d4676061ac2efa96f7323fcce7e2e
- Customs Code
- DHA00601572407
Company information
- Manufacturer
- ARKRAY Factory, Inc., Head office factory
- Manufacturer Country
- Japan
- Authorized Representative
- SYNGEN BIOTECH CO., LTD.
Product details
- Intended Use
- SPOTCHEM II Blood Urea Nitrogen is an in vitro diagnostic test used in serum or plasma for quantitative determination of Blood Urea Nitrogen, which is dedicated to SPOTCHEM instruments.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1770 尿素氮試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Dec 22, 2005
- Expiry Date
- Dec 22, 2025
About this record
Access comprehensive regulatory information for "Arkola" serum urea nitrogen test strip in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 380d4676061ac2efa96f7323fcce7e2e and manufactured by ARKRAY Factory, Inc., Head office factory. The authorized representative in Taiwan is SYNGEN BIOTECH CO., LTD..
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