Taiwan FDA registration 965fd8383d7a8a5240cf30a261a6f241

Nofaferric Anti-Helicobacter pylori Immunoassay Kit (unsterilized)

TW: 諾法鐵抗幽門螺旋桿菌免疫分析套組(未滅菌)

Taiwan·Risk Class 1·GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH·Registered May 23, 2007 – May 23, 2027Active

Registration details

Analysis ID: 965fd8383d7a8a5240cf30a261a6f241
Customs Code: DHA04400589904

Company information

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

Product details

Intended Use: Limited to the classification and grading management of medical devices, the first level identification range of "Helicobacter serum reagent (C.0003)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.0003 螺旋桿菌屬血清試劑
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: May 23, 2007
Expiry Date: May 23, 2027

About this record

Access comprehensive regulatory information for Nofaferric Anti-Helicobacter pylori Immunoassay Kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 965fd8383d7a8a5240cf30a261a6f241 and manufactured by GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

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