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"Camel Kintec" one-use laryngoscope blade (sterilized) - Taiwan Registration f45fd45d3e442b38ffa3a7b4d1f9fb50

Access comprehensive regulatory information for "Camel Kintec" one-use laryngoscope blade (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f45fd45d3e442b38ffa3a7b4d1f9fb50 and manufactured by HENAN TUOREN KINGTAEK MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..

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f45fd45d3e442b38ffa3a7b4d1f9fb50
Registration Details
Taiwan FDA Registration: f45fd45d3e442b38ffa3a7b4d1f9fb50
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Device Details

"Camel Kintec" one-use laryngoscope blade (sterilized)
TW: โ€œ้งไบบ้‡‘ๆณฐๅ…‹โ€ไธ€ๆฌกไฝฟ็”จๅž‹ๅ–‰้ ญ้ก่‘‰็‰‡ (ๆป…่Œ)
Risk Class 1

Registration Details

f45fd45d3e442b38ffa3a7b4d1f9fb50

DHA09600406906

Company Information

Product Details

Limited to the first level identification range of the "rigid laryngoscope (D.5540)" of the Measures for the Classification and Grading Management of Medical Devices.

D Anesthesiology

D.5540 Rigid laryngoscope

Chinese goods;; QMS/QSD;; input

Dates and Status

Jan 07, 2020

Jan 07, 2030