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“GE” Anesthesia System - Taiwan Registration 049e10a12f80282bdbd6711d1abefdcb

Access comprehensive regulatory information for “GE” Anesthesia System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 049e10a12f80282bdbd6711d1abefdcb and manufactured by DATEX-OHMEDA INC.. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, 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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049e10a12f80282bdbd6711d1abefdcb
Registration Details
Taiwan FDA Registration: 049e10a12f80282bdbd6711d1abefdcb
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Device Details

“GE” Anesthesia System
TW: “奇異”麻醉系統
Risk Class 2
MD

Registration Details

049e10a12f80282bdbd6711d1abefdcb

Ministry of Health Medical Device Import No. 028280

DHA05602828001

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

D Devices for anesthesiology

D5160 Anesthetic or analgesic gas supply

Imported from abroad

Dates and Status

Apr 06, 2016

Apr 06, 2026