Taiwan FDA registration ad6001cc2d69d42769e1f92ab39b236b

Oji nose sea nose sprayer

TW: 歐治鼻海水鼻用噴霧器
Taiwan flagTaiwan·Risk Class 2·GSK Consumer Healthcare SARL;; SPPH·Registered Dec 20, 2016 – Dec 20, 2026Active
Registration details
Analysis ID
ad6001cc2d69d42769e1f92ab39b236b
Customs Code
DHA05602922304
Company information
Manufacturer Country
France;;Switzerland
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
G ENT Science
Product Type (Level 2)
G.5220 Ear, nose and throat applicators and substances used in conjunction thereof
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Dec 20, 2016
Expiry Date
Dec 20, 2026
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About this record

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.

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