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"Veili" endotracheal tube - Taiwan Registration cf3446c13edb3076c7e69c7056a7a3bf

Access comprehensive regulatory information for "Veili" 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 cf3446c13edb3076c7e69c7056a7a3bf 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, 1 companies making similar products including Well Lead Medical Co., Ltd., and 3 recent registrations in the same category. 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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cf3446c13edb3076c7e69c7056a7a3bf
Registration Details
Taiwan FDA Registration: cf3446c13edb3076c7e69c7056a7a3bf
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Device Details

"Veili" endotracheal tube
TW: โ€œ็ถญ็ซ‹โ€ๆฐฃ็ฎกๅ…ง็ฎก
Risk Class 2

Registration Details

cf3446c13edb3076c7e69c7056a7a3bf

DHA09200115007

Company Information

Product Details

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

D Anesthesiology

D.5730 Endotracheal tubes

Input;; Chinese goods

Dates and Status

Sep 18, 2020

Sep 18, 2025

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