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"ANEST IWATA" Medical gas Manifolds and Outlet assembly (Non-Sterile) - Taiwan Registration 2335619324ba7df279a55eccd60959aa

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..

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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2335619324ba7df279a55eccd60959aa
Registration Details
Taiwan FDA Registration: 2335619324ba7df279a55eccd60959aa
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Device Details

"ANEST IWATA" Medical gas Manifolds and Outlet assembly (Non-Sterile)
TW: "ๅฒฉ็”ฐ" ้†ซ็”จๆฐฃ้ซ”ๆŽฅ้ ญ็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2335619324ba7df279a55eccd60959aa

Ministry of Health Medical Device Import No. 021557

DHA09402155700

Company Information

Japan

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Medical Gas Connector Group (D.6885)".

D Devices for anesthesiology

D6885 Medical Gas Connector Group

Imported from abroad

Dates and Status

May 22, 2020

May 22, 2025