Taiwan FDA registration abfdb545d4fd48c0f6e9f54566684ae0
"Vibim" laryngeal airway tube (unsterilized)
TW: "維比姆" 喉頭氣道管 (未滅菌)
Taiwan·Risk Class 1·VBM MEDIZINTECHNIK GMBH·Registered Dec 25, 2019 – Dec 25, 2029ActiveRegistration details
- Analysis ID
- abfdb545d4fd48c0f6e9f54566684ae0
- Customs Code
- DHA09402113500
Company information
- Manufacturer
- VBM MEDIZINTECHNIK GMBH
- 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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Dec 25, 2019
- Expiry Date
- Dec 25, 2029
About this record
Access comprehensive regulatory information for "Vibim" laryngeal airway tube (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number abfdb545d4fd48c0f6e9f54566684ae0 and manufactured by VBM MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is GRANDMEDICAL ENTERPRISE LTD..
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