Taiwan FDA registration 74a7e7a9b097c5b279324e412fd2ce1f
"Vibim" endotracheal tube through strip (sterilized)
TW: "維比姆" 氣管內管通條 (滅菌)
Taiwan·Risk Class 1·VBM MEDIZINTECHNIK GMBH·Registered Dec 25, 2019 – Dec 25, 2029ActiveRegistration details
- Analysis ID
- 74a7e7a9b097c5b279324e412fd2ce1f
- Customs Code
- DHA09402113401
Company information
- Manufacturer
- VBM MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- GRANDMEDICAL ENTERPRISE LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "endotracheal tube probe (D.5790)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5790 氣管內管探針
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Dec 25, 2019
- Expiry Date
- Dec 25, 2029
About this record
Access comprehensive regulatory information for "Vibim" endotracheal tube through strip (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 74a7e7a9b097c5b279324e412fd2ce1f and manufactured by VBM MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is GRANDMEDICAL ENTERPRISE LTD..
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