Taiwan FDA registration 3c6c13d74fdef0e5848ab1b1117734e9
"Siemens" gram-negative urine synergistic composite test group five
TW: “西門子”革蘭氏陰性尿液協同複合檢驗組五型
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Jun 18, 2012 – Jun 18, 2017CancelledRegistration details
- Analysis ID
- 3c6c13d74fdef0e5848ab1b1117734e9
- Customs Code
- DHA00602365408
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS INC.
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS LIMITED
Product details
- Intended Use
- For the qualitative and/or quantitative determination of antimicrobial resistance in fast-growing aerobic and facultative anaerobic gram-negative bacilli, and/or to identify strains.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.1645 Automatic Antibiotic Sensitivity Test System for Short Incubation Period
- Import Information
- import
Dates and status
- Registration Date
- Jun 18, 2012
- Expiry Date
- Jun 18, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Siemens" gram-negative urine synergistic composite test group five in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3c6c13d74fdef0e5848ab1b1117734e9 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS LIMITED.
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