Taiwan FDA registration 66d846ba26ba939ff4b7a74af1593c2f
“Atos” Provox LaryTube (Non-Sterile)
TW: “雅多司”普羅適喉切套管(未滅菌)
Taiwan·Risk Class 1·MD·Atos Medical AB·Registered Feb 26, 2019 – Feb 26, 2024ExpiredRegistration details
- Analysis ID
- 66d846ba26ba939ff4b7a74af1593c2f
- License Form
- Ministry of Health Medical Device Import No. 020129
- Customs Code
- DHA09402012900
Company information
- Manufacturer
- Atos Medical AB
- Manufacturer Country
- Sweden
- Authorized Representative
- WHOLE WELL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Laryngeal Supplement (Taub Type) (G.3730)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G3730 Throat Supplement (Taub type)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 26, 2019
- Expiry Date
- Feb 26, 2024
About this record
Access comprehensive regulatory information for “Atos” Provox LaryTube (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 66d846ba26ba939ff4b7a74af1593c2f and manufactured by Atos Medical AB. The authorized representative in Taiwan is WHOLE WELL CO., LTD..
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