Taiwan FDA registration 691546f95ee86ace86dd3406dd78261f

"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 Oct 24, 2019 – Oct 24, 2029Active
Registration details
Analysis ID
691546f95ee86ace86dd3406dd78261f
Customs Code
DHA09402097602
Company information
Manufacturer Country
Germany
Authorized Representative
GRANDMEDICAL ENTERPRISE LTD.
Product details
Intended Use
Limited to the classification and grading management method of medical equipment, oropharyngeal airway canal (D.5110) first grade identification range.
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
Oct 24, 2019
Expiry Date
Oct 24, 2029
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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 691546f95ee86ace86dd3406dd78261f 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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