Taiwan FDA registration cc4de63cfdab7b10781f26886d936bea

IMMULITE/IMMULITE 1000 IL-6

TW: 免疫特介白素-6檢驗試劑組

Taiwan·Risk Class 2·MD·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED·Registered Aug 15, 2013 – Aug 15, 2028Active

Registration details

Analysis ID: cc4de63cfdab7b10781f26886d936bea
License Form: Ministry of Health Medical Device Import No. 025264
Customs Code: DHA05602526401

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 with IMMULITE and IMMULITE 1000 analysis systems to quantitatively detect serum, EDTA or heparinized plasma mediation-6 (IL-6) concentrations.
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C3210 Endotoxin Analysis Reagent
Import Information: Imported from abroad

Dates and status

Registration Date: Aug 15, 2013
Expiry Date: Aug 15, 2028

About this record

Access comprehensive regulatory information for IMMULITE/IMMULITE 1000 IL-6 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cc4de63cfdab7b10781f26886d936bea and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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