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"GI Supply" H. Pylori Test ( Non-Sterile) - Taiwan Registration a82078dd3646b3fc77b2f86ad2ab616c

Access comprehensive regulatory information for "GI Supply" H. Pylori Test ( Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a82078dd3646b3fc77b2f86ad2ab616c and manufactured by GI SUPPLY. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).

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a82078dd3646b3fc77b2f86ad2ab616c
Registration Details
Taiwan FDA Registration: a82078dd3646b3fc77b2f86ad2ab616c
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Device Details

"GI Supply" H. Pylori Test ( Non-Sterile)
TW: "ๅ‰ๆ„›" ๅนฝ้–€่žบๆ—‹ๆกฟ่Œ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

a82078dd3646b3fc77b2f86ad2ab616c

Department of Health Medical Device Import No. 009955

DHA04400995508

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Identification and Measurement Equipment (C.2660)".

C Immunology and microbiology devices

C0003 Helicobacter serological reagent

Imported from abroad

Dates and Status

Mar 01, 2011

Mar 01, 2026