Taiwan FDA registration 7e57eb9a08627ae8ba1f6eb0e579032d

"Veili" endotracheal tube

TW: “維立”氣管內管
Taiwan flagTaiwan·Risk Class 2·Well Lead Medical Co., Ltd.·Registered Dec 03, 2019 – Dec 03, 2029Active
Registration details
Analysis ID
7e57eb9a08627ae8ba1f6eb0e579032d
Customs Code
DHA09200108802
Company information
Manufacturer Country
China
Authorized Representative
TAIWAN MEDICAL SERVICES CORPORATION
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5730 Endotracheal tubes
Import Information
Chinese goods;; input
Dates and status
Registration Date
Dec 03, 2019
Expiry Date
Dec 03, 2029
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About this record

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 7e57eb9a08627ae8ba1f6eb0e579032d 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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