Oji nose sea nose sprayer - Taiwan Registration ad6001cc2d69d42769e1f92ab39b236b
Access comprehensive regulatory information for Oji nose sea nose sprayer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ad6001cc2d69d42769e1f92ab39b236b and manufactured by GSK Consumer Healthcare SARL;; SPPH. The authorized representative in Taiwan is HALEON UK SERVICES LIMITED TAIWAN BRANCH.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including NOVARTIS CONSUMER HEALTH SA;; SPPH, 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
Registration Details
ad6001cc2d69d42769e1f92ab39b236b
DHA05602922304
Product Details
For details, it is Chinese approved copy of the imitation order
G ENT Science
G.5220 Ear, nose and throat applicators and substances used in conjunction thereof
Contract manufacturing;; input
Dates and Status
Dec 20, 2016
Dec 20, 2026

