"Bien Air" Ear, nose, and throat bur (Non-Sterile)
Taiwan·Risk Class 1·MD·BIEN AIR SURGERY SA·Registered Aug 07, 2014 – Aug 07, 2019Cancelled- Analysis ID
- 26999cde73b438d4d833e661b595781a
- License Form
- Ministry of Health Medical Device Import No. 014418
- Customs Code
- DHA09401441808
- Manufacturer
- BIEN AIR SURGERY SA
- Manufacturer Country
- Switzerland
- Authorized Representative
- Chenyu Technology Co., Ltd
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4140 Round hammer for otolaryngology
- Import Information
- Imported from abroad
- Registration Date
- Aug 07, 2014
- Expiry Date
- Aug 07, 2019
- Cancellation Date
- Jun 22, 2022
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Bien Air" Ear, nose, and throat bur (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 26999cde73b438d4d833e661b595781a and manufactured by BIEN AIR SURGERY SA. The authorized representative in Taiwan is Chenyu Technology Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BIEN AIR SURGERY SA, 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.