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"Veli" single-use with suction tube, endotracheal tube - Taiwan Registration a2c8165f3aedf17dd030bd9db82dd36b

Access comprehensive regulatory information for "Veli" single-use with suction tube, endotracheal tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a2c8165f3aedf17dd030bd9db82dd36b 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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a2c8165f3aedf17dd030bd9db82dd36b
Registration Details
Taiwan FDA Registration: a2c8165f3aedf17dd030bd9db82dd36b
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Device Details

"Veli" single-use with suction tube, endotracheal tube
TW: โ€œ็ถญ็ซ‹โ€ไธ€ๆฌกๆ€งไฝฟ็”จๅธถๆŠฝ็—ฐ็ฎกๆฐฃ็ฎกๅ…ง็ฎก
Risk Class 2

Registration Details

a2c8165f3aedf17dd030bd9db82dd36b

DHA09200110400

Company Information

Product Details

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

D Anesthesiology

D.5730 Endotracheal tubes

Chinese goods;; input

Dates and Status

Jan 16, 2020

Jan 16, 2025