Taiwan FDA registration 2335619324ba7df279a55eccd60959aa

"ANEST IWATA" Medical gas Manifolds and Outlet assembly (Non-Sterile)

TW: "岩田" 醫用氣體接頭組 (未滅菌)

Taiwan·Risk Class 1·MD·KOMATSU-SEIKI CO.,LTD.·Registered May 22, 2020 – May 22, 2025Expired

Registration details

Analysis ID: 2335619324ba7df279a55eccd60959aa
License Form: Ministry of Health Medical Device Import No. 021557
Customs Code: DHA09402155700

Company information

Manufacturer: KOMATSU-SEIKI CO.,LTD.
Manufacturer Country: Japan
Authorized Representative: JING YE ENGINEERING CO.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Medical Gas Connector Group (D.6885)".
Product Type (Level 1): D Devices for anesthesiology
Product Type (Level 2): D6885 Medical Gas Connector Group
Import Information: Imported from abroad

Dates and status

Registration Date: May 22, 2020
Expiry Date: May 22, 2025

About this record

Access comprehensive regulatory information for "ANEST IWATA" Medical gas Manifolds and Outlet assembly (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 2335619324ba7df279a55eccd60959aa and manufactured by KOMATSU-SEIKI CO.,LTD.. The authorized representative in Taiwan is JING YE ENGINEERING CO..

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