Taiwan FDA registration 2dce3faba7edec1c55c69098906703aa

Baijie Helicobacter pylori IgM enzyme immunoassay group (unsterilized)

TW: 佰杰幽門螺旋桿菌IgM酵素免疫分析組(未滅菌)

Taiwan·Risk Class 1·BIOCHECK, INC.·Registered May 25, 2007 – May 25, 2027Active

Registration details

Analysis ID: 2dce3faba7edec1c55c69098906703aa
Customs Code: DHA04400590703

Company information

Manufacturer: BIOCHECK, INC.
Manufacturer Country: United States
Authorized Representative: GENERAL BIOLOGICALS CORP.

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: import

Dates and status

Registration Date: May 25, 2007
Expiry Date: May 25, 2027

About this record

Access comprehensive regulatory information for Baijie Helicobacter pylori IgM enzyme immunoassay group (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2dce3faba7edec1c55c69098906703aa and manufactured by BIOCHECK, INC.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

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