Taiwan FDA registration 4adc22c2f70324c451dcb1cc952e7174

"Jiai" Helicobacter pylori reagent (unsterilized)

TW: "吉愛" 幽門螺旋桿菌試劑 (未滅菌)

Taiwan·Risk Class 1·GI SUPPLY·Registered Mar 01, 2011 – Mar 01, 2026Expired

Registration details

Analysis ID: 4adc22c2f70324c451dcb1cc952e7174
Customs Code: DHA04400995508

Company information

Manufacturer: GI SUPPLY
Manufacturer Country: United States
Authorized Representative: Tronmed CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Classification and Grading of Medical Devices "Microbial Identification and Determination Equipment (C.2660)".
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 01, 2011
Expiry Date: Mar 01, 2026

About this record

Access comprehensive regulatory information for "Jiai" Helicobacter pylori reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4adc22c2f70324c451dcb1cc952e7174 and manufactured by GI SUPPLY. The authorized representative in Taiwan is Tronmed CO., LTD..

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.