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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.

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ad6001cc2d69d42769e1f92ab39b236b
Registration Details
Taiwan FDA Registration: ad6001cc2d69d42769e1f92ab39b236b
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Device Details

Oji nose sea nose sprayer
TW: ๆญๆฒป้ผปๆตทๆฐด้ผป็”จๅ™ด้œงๅ™จ
Risk Class 2

Registration Details

ad6001cc2d69d42769e1f92ab39b236b

DHA05602922304

Company Information

France;;Switzerland

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

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