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"Hongkang" endotracheal probe (unsterilized) - Taiwan Registration ad3c45c819e16fe3ee514520d858dfcf

Access comprehensive regulatory information for "Hongkang" 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 ad3c45c819e16fe3ee514520d858dfcf and manufactured by Ciguang Technology Co., Ltd. The authorized representative in Taiwan is MEDLUME SCIENTIFIC 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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ad3c45c819e16fe3ee514520d858dfcf
Registration Details
Taiwan FDA Registration: ad3c45c819e16fe3ee514520d858dfcf
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Device Details

"Hongkang" endotracheal probe (unsterilized)
TW: โ€œๅผ˜ๅบทโ€ๆฐฃ็ฎกๅ…ง็ฎกๆŽข้‡(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

ad3c45c819e16fe3ee514520d858dfcf

Company Information

Taiwan, Province of China

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‡

Contract manufacturing;; Domestic

Dates and Status

Feb 14, 2012

Feb 14, 2017

Nov 04, 2019

Cancellation Information

Logged out

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