Oji nose sea nose sprayer (unsterilized) - Taiwan Registration cbcf27483e15ad5bc1d9f3f8359bd9cc
Access comprehensive regulatory information for Oji nose sea nose sprayer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cbcf27483e15ad5bc1d9f3f8359bd9cc and manufactured by NOVARTIS CONSUMER HEALTH SA;; SPPH. The authorized representative in Taiwan is HALEON UK SERVICES LIMITED TAIWAN BRANCH.
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.
Device Details
Registration Details
cbcf27483e15ad5bc1d9f3f8359bd9cc
DHA04400905702
Product Details
Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "ENT Dispensing Devices (G.5220)".
G ENT Science
G.5220 Ear, nose and throat applicators and substances used in conjunction thereof
import
Dates and Status
Aug 09, 2010
Aug 09, 2020
Jun 07, 2022
Cancellation Information
Logged out
่จฑๅฏ่ญๅทฒ้พๆๆๆ