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"Velit" single-lumen endobronchial tube is used at one time - Taiwan Registration 7d93d94fb94a8685dedbebf422c88dee

Access comprehensive regulatory information for "Velit" single-lumen endobronchial tube is used at one time in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7d93d94fb94a8685dedbebf422c88dee 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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7d93d94fb94a8685dedbebf422c88dee
Registration Details
Taiwan FDA Registration: 7d93d94fb94a8685dedbebf422c88dee
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Device Details

"Velit" single-lumen endobronchial tube is used at one time
TW: โ€œ็ถญ็ซ‹โ€ไธ€ๆฌกๆ€งไฝฟ็”จๅ–ฎ่…”ๆ”ฏๆฐฃ็ฎกๅ…ง็ฎก
Risk Class 2

Registration Details

7d93d94fb94a8685dedbebf422c88dee

DHA09200109907

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

D Anesthesiology

D.5740 Gas pipe/bronchi divergence gas line

Chinese goods;; input

Dates and Status

Jan 03, 2020

Jan 03, 2025