Taiwan FDA registration f0fac8ad89c58958e3da604644e96674
Renbara urea nitrogen test system
TW: 篠原尿素氮試驗系統
Taiwan·Risk Class 2·SHINO-TEST CORPORATION, SAGAMIHARA PRODUCTION CENTER·Registered Aug 23, 2012 – Aug 23, 2027ActiveRegistration details
- Analysis ID
- f0fac8ad89c58958e3da604644e96674
- Customs Code
- DHA00602398900
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- Quantitative detection of urea nitrogen in human serum, plasma or urine, dedicated to the Hitachi LABOSPECT system.
- 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
- Aug 23, 2012
- Expiry Date
- Aug 23, 2027
About this record
Access comprehensive regulatory information for Renbara urea nitrogen test system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f0fac8ad89c58958e3da604644e96674 and manufactured by SHINO-TEST CORPORATION, SAGAMIHARA PRODUCTION CENTER. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices