Taiwan FDA registration 1c6f9acb2a6b0203bad5a12b1bce9fbb

"Elgen" atomization treatment system

TW: “愛爾真”霧化治療系統

Taiwan·Risk Class 2·Aerogen Ltd., M&M Qualtech Ltd.; Aerogen Ltd.·Registered Jun 22, 2016 – Jun 22, 2026Expired

Registration details

Analysis ID: 1c6f9acb2a6b0203bad5a12b1bce9fbb
Customs Code: DHA05602861302

Company information

Manufacturer: Aerogen Ltd., M&M Qualtech Ltd.; Aerogen Ltd.
Manufacturer Country: Ireland
Authorized Representative: TRANSCORE TAIWAN CO., LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5630 Nebulizer
Import Information: import

Dates and status

Registration Date: Jun 22, 2016
Expiry Date: Jun 22, 2026

About this record

Access comprehensive regulatory information for "Elgen" atomization treatment system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1c6f9acb2a6b0203bad5a12b1bce9fbb and manufactured by Aerogen Ltd., M&M Qualtech Ltd.; Aerogen Ltd.. The authorized representative in Taiwan is TRANSCORE TAIWAN CO., LTD..

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