Taiwan FDA registration eee607c3c655dda3070a1bac452938e3

Nofafer Human Antigondiformis Immunoglobulin G Enzyme Immunoassay Kit

TW: 諾法鐵人類抗弓漿蟲免疫球蛋白G酵素免疫分析套組

Taiwan·Risk Class 2·GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH·Registered Aug 31, 2006 – Aug 31, 2026Active

Registration details

Analysis ID: eee607c3c655dda3070a1bac452938e3
Customs Code: DHA00601730408

Company information

Manufacturer: GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH
Manufacturer Country: Germany
Authorized Representative: EVERLIGHT BIOTECH(TAIWAN) CO., LTD.

Product details

Intended Use: The Norfa Anti-Toxoplasmin Immunoglobulin G Enzyme Immunoassay Kit is used for the qualitative and quantitative detection of anti-Toxoplasma human immunoglobulin G typing antibodies in human serum or plasma.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3780 弓漿蟲血清試劑
Import Information: import

Dates and status

Registration Date: Aug 31, 2006
Expiry Date: Aug 31, 2026

About this record

Access comprehensive regulatory information for Nofafer Human Antigondiformis Immunoglobulin G Enzyme Immunoassay Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number eee607c3c655dda3070a1bac452938e3 and manufactured by GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

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