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“Spacelabs” Arkon Anesthesia System - Taiwan Registration 83ed0ecce6c16966960dd6b0b0a71a12

Access comprehensive regulatory information for “Spacelabs” Arkon 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 83ed0ecce6c16966960dd6b0b0a71a12 and manufactured by Spacelabs Healthcare Inc.. The authorized representative in Taiwan is CHARITY PHARMACEUTICAL CO., 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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83ed0ecce6c16966960dd6b0b0a71a12
Registration Details
Taiwan FDA Registration: 83ed0ecce6c16966960dd6b0b0a71a12
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Device Details

“Spacelabs” Arkon Anesthesia System
TW: “斯貝司”愛康麻醉系統
Risk Class 2
MD
Cancelled

Registration Details

83ed0ecce6c16966960dd6b0b0a71a12

Ministry of Health Medical Device Import No. 027620

DHA05602762004

Company Information

United States

Product Details

D Devices for anesthesiology

D5160 Anesthetic or analgesic gas supply

Imported from abroad

Dates and Status

Sep 04, 2015

Sep 04, 2020

Sep 29, 2021

Cancellation Information

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