Taiwan FDA registration 8e89e41441140d7680a42355b60d2ad2
"Siemens" N homocysteine latex reagent
TW: “西門子”N同半胱氨酸 乳膠試劑
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Registered Nov 01, 2011 – Nov 01, 2026ActiveRegistration details
- Analysis ID
- 8e89e41441140d7680a42355b60d2ad2
- Customs Code
- DHA00602273605
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- Homocysteine concentrations in human serum, heparin plasma and EDTA plasma were quantified by particle enhanced immunoturbidimetry and used with BN*II and BN ProSpec System.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1377 Cystine-like non-quantitative testing system in urine
- Import Information
- import
Dates and status
- Registration Date
- Nov 01, 2011
- Expiry Date
- Nov 01, 2026
About this record
Access comprehensive regulatory information for "Siemens" N homocysteine latex reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8e89e41441140d7680a42355b60d2ad2 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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