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"Vibim" oropharyngeal airway tube (sterilized) - Taiwan Registration 1df15317a3d13d811d47c2c689c32118

Access comprehensive regulatory information for "Vibim" oropharyngeal airway tube (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1df15317a3d13d811d47c2c689c32118 and manufactured by VBM MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is GRANDMEDICAL ENTERPRISE LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including VBM MEDIZINTECHNIK GMBH, and 1 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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1df15317a3d13d811d47c2c689c32118
Registration Details
Taiwan FDA Registration: 1df15317a3d13d811d47c2c689c32118
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Device Details

"Vibim" oropharyngeal airway tube (sterilized)
TW: "็ถญๆฏ”ๅง†"ๅฃๅ’ฝๆฐฃ้“็ฎก(ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

1df15317a3d13d811d47c2c689c32118

DHA09401397203

Company Information

Germany

Product Details

Limited to the first level recognition range of the oropharyngeal airway tube (D.5110) for the management of medical devices.

D Anesthesiology

D.5110 Oropharyngeal airway tubes

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Mar 19, 2014

Mar 19, 2019

Aug 05, 2022

Cancellation Information

Logged out

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