Taiwan FDA registration ecf344a97b02758179855e0f61655768
IMMULITE 2000 Estradiol
TW: 免疫特2000雌二醇試驗系統
Taiwan·Risk Class 2·MD·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED·Registered Jun 28, 2018 – Jun 28, 2028ActiveRegistration details
- Analysis ID
- ecf344a97b02758179855e0f61655768
- License Form
- Ministry of Health Medical Device Import No. 031310
- Customs Code
- DHA05603131004
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- This product is used in the IMMULITE 2000 system for the quantitative analysis of estradiol content (estradiol-17 β, E2) in serum.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1260 Estradiol Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 28, 2018
- Expiry Date
- Jun 28, 2028
About this record
Access comprehensive regulatory information for IMMULITE 2000 Estradiol in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ecf344a97b02758179855e0f61655768 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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