Taiwan FDA registration 4182f0d0749ad103d1dbd9b1cc0b6c48

"Liming" H. pylori Test (Non-Sterile)

TW: "利明" 幽門桿菌檢驗試劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·NANJING LIMING BIO-PRODUCTS CO., LTD.·Registered Jul 03, 2015 – Jul 03, 2020Cancelled
Registration details
Analysis ID
4182f0d0749ad103d1dbd9b1cc0b6c48
License Form
Ministry of Health Medical Device Land Transport No. 002445
Customs Code
DHA09600244501
Company information
Manufacturer Country
China
Authorized Representative
LIKWANG INSTRUMENTS CO., LTD.
Product details
Product Type (Level 1)
C Immunology and microbiology devices
Product Type (Level 2)
C0003 Helicobacter serological reagent
Import Information
Imported from abroad; Made in China
Dates and status
Registration Date
Jul 03, 2015
Expiry Date
Jul 03, 2020
Cancellation Date
Jun 22, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Liming" 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 4182f0d0749ad103d1dbd9b1cc0b6c48 and manufactured by NANJING LIMING BIO-PRODUCTS CO., LTD.. The authorized representative in Taiwan is LIKWANG INSTRUMENTS 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.

Free DatabasePowered by Pure Global AI89,000+ Devices