Taiwan FDA registration 1df15317a3d13d811d47c2c689c32118

"Vibim" oropharyngeal airway tube (sterilized)

TW: "維比姆"口咽氣道管(滅菌)
Taiwan flagTaiwan·Risk Class 1·VBM MEDIZINTECHNIK GMBH·Registered Mar 19, 2014 – Mar 19, 2019Cancelled
Registration details
Analysis ID
1df15317a3d13d811d47c2c689c32118
Customs Code
DHA09401397203
Company information
Manufacturer Country
Germany
Authorized Representative
GRANDMEDICAL ENTERPRISE LTD.
Product details
Intended Use
Limited to the first level recognition range of the oropharyngeal airway tube (D.5110) for the management of medical devices.
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5110 Oropharyngeal airway tubes
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Mar 19, 2014
Expiry Date
Mar 19, 2019
Cancellation Date
Aug 05, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

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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