Taiwan FDA registration 76eea1b73ced174c2335723bc4bd9e75

"Probiotic" pylori reagents

TW: "益生"幽門桿菌試劑
Taiwan flagTaiwan·Risk Class 1·MD BIOTECH CORPORATION·Registered Mar 14, 2006 – Mar 14, 2016Cancelled
Registration details
Analysis ID
76eea1b73ced174c2335723bc4bd9e75
Customs Code
DHA04400293506
Company information
Manufacturer Country
United States
Authorized Representative
Yisheng Technology Co., Ltd
Product details
Intended Use
Rapid identification of urea content of Helicobacter pylori in samples.
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
Mar 14, 2006
Expiry Date
Mar 14, 2016
Cancellation Date
Apr 25, 2018
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for "Probiotic" pylori reagents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 76eea1b73ced174c2335723bc4bd9e75 and manufactured by MD BIOTECH CORPORATION. The authorized representative in Taiwan is Yisheng Technology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MD BIOTECH CORPORATION, and 1 recent registrations in the same category. 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.

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