Taiwan FDA registration 79ae31aee0fb8bc72d1b90577a0b9f69
"Wanfu" Helicobacter pylori antibody test strip (whole blood/serum/plasma) (unsterilized)
TW: “萬孚”幽門螺旋桿菌抗體檢測試紙 (全血/血清/血漿) (未滅菌)
Registration details
- Analysis ID
- 79ae31aee0fb8bc72d1b90577a0b9f69
- Customs Code
- DHA09600359509
Company information
- Manufacturer
- GUANGZHOU WONDFO BIOTECH CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
Product details
- Intended Use
- Limited to the classification and grading management of medical devices, the first level identification range of "Helicobacter serum 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
- Chinese goods;; input
Dates and status
- Registration Date
- Nov 12, 2018
- Expiry Date
- Nov 12, 2023
About this record
Access comprehensive regulatory information for "Wanfu" Helicobacter pylori antibody test strip (whole blood/serum/plasma) (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 79ae31aee0fb8bc72d1b90577a0b9f69 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