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"Genejet" NASAL ASPIRATOR (Non-Sterile) - Taiwan Registration 9b5fe6e592352443b3bbeed87239fd45

Access comprehensive regulatory information for "Genejet" NASAL ASPIRATOR (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9b5fe6e592352443b3bbeed87239fd45 and manufactured by NASALPODUKTER SVERIGE AB. The authorized representative in Taiwan is GENEJET BIOTECH CO., LTD..

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.

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9b5fe6e592352443b3bbeed87239fd45
Registration Details
Taiwan FDA Registration: 9b5fe6e592352443b3bbeed87239fd45
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Device Details

"Genejet" NASAL ASPIRATOR (Non-Sterile)
TW: "ๅ‹ๆท"ๅธ้ผปๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

9b5fe6e592352443b3bbeed87239fd45

Ministry of Health Medical Device Import No. 015179

DHA09401517908

Company Information

Sweden

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Power Nasal Irrigator (G.5550)".

G ENT device

G5550 powered nose irrigator

Imported from abroad

Dates and Status

Apr 29, 2015

Apr 29, 2025