Taiwan FDA registration 9b5fe6e592352443b3bbeed87239fd45

"Genejet" NASAL ASPIRATOR (Non-Sterile)

TW: "勁捷"吸鼻器(未滅菌)

Taiwan·Risk Class 1·MD·NASALPODUKTER SVERIGE AB·Registered Apr 29, 2015 – Apr 29, 2025Expired

Registration details

Analysis ID: 9b5fe6e592352443b3bbeed87239fd45
License Form: Ministry of Health Medical Device Import No. 015179
Customs Code: DHA09401517908

Company information

Manufacturer: NASALPODUKTER SVERIGE AB
Manufacturer Country: Sweden
Authorized Representative: GENEJET BIOTECH CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Power Nasal Irrigator (G.5550)".
Product Type (Level 1): G ENT device
Product Type (Level 2): G5550 powered nose irrigator
Import Information: Imported from abroad

Dates and status

Registration Date: Apr 29, 2015
Expiry Date: Apr 29, 2025

About this record

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..

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