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"Hongan" endotracheal probe (unsterilized) - Taiwan Registration 52e3d0fe4e62f57f0b1e42d27058d8ef

Access comprehensive regulatory information for "Hongan" endotracheal probe (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 52e3d0fe4e62f57f0b1e42d27058d8ef and manufactured by HONG AN MEDICAL APPLIANCE CO., LTD.. The authorized representative in Taiwan is SHAN-LUEN MEDICAL 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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52e3d0fe4e62f57f0b1e42d27058d8ef
Registration Details
Taiwan FDA Registration: 52e3d0fe4e62f57f0b1e42d27058d8ef
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Device Details

"Hongan" endotracheal probe (unsterilized)
TW: "ๅฎๅฎ‰" ๆฐฃ็ฎกๅ…ง็ฎกๆŽข้‡ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

52e3d0fe4e62f57f0b1e42d27058d8ef

DHA04600160002

Company Information

Product Details

Limited to the first level recognition range of endotracheal tube probe (D.5790) of the management method for medical equipment.

D Anesthesiology

D.5790 ๆฐฃ็ฎกๅ…ง็ฎกๆŽข้‡

Input;; Chinese goods

Dates and Status

Mar 06, 2012

Mar 06, 2022

Apr 12, 2024

Cancellation Information

Logged out

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