Taiwan FDA registration f7ed115f6e17d17cd398df4a2f83f5cf
Immunogastrin test group
TW: 免疫特胃泌素試驗組
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED·Registered May 10, 2012 – May 10, 2022CancelledRegistration details
- Analysis ID
- f7ed115f6e17d17cd398df4a2f83f5cf
- Customs Code
- DHA00602348001
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- This product needs to be used with IMMULITE and IMMULITE 1000 analyzers to quantitatively detect the concentration of gastrin in serum.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1325 胃泌素試驗系統
- Import Information
- import
Dates and status
- Registration Date
- May 10, 2012
- Expiry Date
- May 10, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Immunogastrin test group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f7ed115f6e17d17cd398df4a2f83f5cf and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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