Taiwan FDA registration 1f4da0b41f0ec2bd4929c64631e93d5b
"Siemens" Blood Gas Control (Non-Sterile)
TW: "西門子" 血液氣體品管液 (未滅菌)
Taiwan·Risk Class 1·MD·BIONOSTICS INC.·Registered Aug 10, 2017 – Aug 10, 2027ActiveRegistration details
- Analysis ID
- 1f4da0b41f0ec2bd4929c64631e93d5b
- License Form
- Ministry of Health Medical Device Import No. 018167
- Customs Code
- DHA09401816703
Company information
- Manufacturer
- BIONOSTICS INC.
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1660 Quality Control Materials (Analytical and Non-Analytical)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 10, 2017
- Expiry Date
- Aug 10, 2027
About this record
Access comprehensive regulatory information for "Siemens" Blood Gas Control (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1f4da0b41f0ec2bd4929c64631e93d5b and manufactured by BIONOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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