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"Boehringer" Rebreathing device (Non-Sterile) - Taiwan Registration e3b4beef93bb9fe614ef12104298617c

Access comprehensive regulatory information for "Boehringer" Rebreathing device (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 e3b4beef93bb9fe614ef12104298617c and manufactured by Boehringer Laboratories, LLC. The authorized representative in Taiwan is NSH MEDICAL CORP..

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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e3b4beef93bb9fe614ef12104298617c
Registration Details
Taiwan FDA Registration: e3b4beef93bb9fe614ef12104298617c
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Device Details

"Boehringer" Rebreathing device (Non-Sterile)
TW: "ๅฏถ้ˆๆ ผ"ๅ†ๅธๅ…ฅ่ฃ็ฝฎ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

e3b4beef93bb9fe614ef12104298617c

Ministry of Health Medical Device Import No. 014559

DHA09401455900

Company Information

United States

Product Details

D Devices for anesthesiology

D5675 Reinhalation device

Imported from abroad

Dates and Status

Oct 13, 2014

Oct 13, 2019

May 19, 2022

Cancellation Information

Logged out

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