Taiwan FDA registration 9e46feb14f981f9b7164ed0e61203f79
“Vyaire” Pulmonary Function Test System
TW: “維亞爾” 肺功能測試系統
Taiwan·Risk Class 2·MD·Vyaire Medical GmbH·Registered Mar 30, 2021 – Mar 30, 2026ExpiredRegistration details
- Analysis ID
- 9e46feb14f981f9b7164ed0e61203f79
- License Form
- Ministry of Health Medical Device Import No. 034478
- Customs Code
- DHA05603447805
Company information
- Manufacturer
- Vyaire Medical GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- BIOSYSTEMS INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D1840 Spirometer for diagnosis
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 30, 2021
- Expiry Date
- Mar 30, 2026
About this record
Access comprehensive regulatory information for “Vyaire” Pulmonary Function Test System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9e46feb14f981f9b7164ed0e61203f79 and manufactured by Vyaire Medical GmbH. The authorized representative in Taiwan is BIOSYSTEMS INC..
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