Taiwan FDA registration c6320f3f1573d9d9d4cd5cd5fe85bd4a

"Wanfu" Helicobacter pylori test kit (unsterilized)

TW: “萬孚”幽門螺旋桿菌檢測試劑盒(未滅菌)
Taiwan flagTaiwan·Risk Class 1·GUANGZHOU WONDFO BIOTECH CO., LTD.·Registered Jan 27, 2011 – Jan 27, 2021Cancelled
Registration details
Analysis ID
c6320f3f1573d9d9d4cd5cd5fe85bd4a
Customs Code
DHA04600127004
Company information
Manufacturer Country
China
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
Input;; Chinese goods
Dates and status
Registration Date
Jan 27, 2011
Expiry Date
Jan 27, 2021
Cancellation Date
Aug 15, 2023
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Wanfu" Helicobacter pylori test 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 c6320f3f1573d9d9d4cd5cd5fe85bd4a and manufactured by GUANGZHOU WONDFO BIOTECH CO., LTD.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free DatabasePowered by Pure Global AI89,000+ Devices