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"Veali" endotracheal probe (sterilized/unsterilized) - Taiwan Registration 3d175bdb62e97a610f8e5b1ed3aec66e

Access comprehensive regulatory information for "Veali" endotracheal probe (sterilized/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3d175bdb62e97a610f8e5b1ed3aec66e and manufactured by Well Lead Medical Co., Ltd.. The authorized representative in Taiwan is TAIWAN MEDICAL SERVICES CORPORATION.

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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3d175bdb62e97a610f8e5b1ed3aec66e
Registration Details
Taiwan FDA Registration: 3d175bdb62e97a610f8e5b1ed3aec66e
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Device Details

"Veali" endotracheal probe (sterilized/unsterilized)
TW: "็ถญ็ซ‹" ๆฐฃ็ฎกๅ…ง็ฎกๆŽข้‡ (ๆป…่Œ/ๆœชๆป…่Œ)
Risk Class 1

Registration Details

3d175bdb62e97a610f8e5b1ed3aec66e

DHA09600370108

Company Information

Product Details

Limited to the first level identification range of the "endotracheal tube probe (D.5790)" of the Measures for the Classification and Grading Management of Medical Equipment.

D Anesthesiology

D.5790 ๆฐฃ็ฎกๅ…ง็ฎกๆŽข้‡

Chinese goods;; QMS/QSD;; input

Dates and Status

Feb 27, 2019

Feb 27, 2029