"Vibim" oropharyngeal airway tube (sterilized)
- Analysis ID
- 1df15317a3d13d811d47c2c689c32118
- Customs Code
- DHA09401397203
- Manufacturer
- VBM MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- GRANDMEDICAL ENTERPRISE LTD.
- 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
- Registration Date
- Mar 19, 2014
- Expiry Date
- Mar 19, 2019
- Cancellation Date
- Aug 05, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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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.