Abbott high-risk human papillomavirus test kit - Taiwan Registration ac2da981a8facf20035e751518c0841a
Access comprehensive regulatory information for Abbott high-risk human papillomavirus test kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number ac2da981a8facf20035e751518c0841a and manufactured by ABBOTT GMBH & CO. Medical history. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ABBOTT MOLECULAR INC., and 1 recent registrations in the same category. 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.
Device Details
Product Details
The Abbott High-Risk HPV Test Kit is an external qualitative test that detects the presence of DNA from high-risk HPV in clinical specimens (including 14 genotypes: 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68). New performance (specification: 02N09-092): As detailed in the Chinese copy of the copy.
C Immunology and microbiology
C.0004 Human papillomavirus serum reagent
import
Dates and Status
Sep 04, 2012
Sep 04, 2027