Taiwan FDA registration 77660f753322067cd9bcee1095dfcefe

Baijie Helicobacter pylori IgA enzyme immunoassay group

TW: 佰杰幽門螺旋桿菌IgA酵素免疫分析組

Taiwan·Risk Class 1·BIOCHECK, INC.·Registered May 25, 2007 – May 25, 2012Cancelled

Registration details

Analysis ID: 77660f753322067cd9bcee1095dfcefe
Customs Code: DHA04400590805

Company information

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

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Helicobacter Serological 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, 2012
Cancellation Date: May 05, 2014

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Baijie Helicobacter pylori IgA enzyme immunoassay group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 77660f753322067cd9bcee1095dfcefe and manufactured by BIOCHECK, INC.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

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