Taiwan FDA registration a82078dd3646b3fc77b2f86ad2ab616c
"GI Supply" H. Pylori Test ( Non-Sterile)
TW: "吉愛" 幽門螺旋桿菌試劑 (未滅菌)
Taiwan·Risk Class 1·MD·GI SUPPLY·Registered Mar 01, 2011 – Mar 01, 2026ExpiredRegistration details
- Analysis ID
- a82078dd3646b3fc77b2f86ad2ab616c
- License Form
- Department of Health Medical Device Import No. 009955
- Customs Code
- DHA04400995508
Company information
- Manufacturer
- GI SUPPLY
- Manufacturer Country
- United States
- Authorized Representative
- IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG)
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Identification and Measurement Equipment (C.2660)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C0003 Helicobacter serological reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 01, 2011
- Expiry Date
- Mar 01, 2026
About this record
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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