Taiwan FDA registration dae576848c521f60990c8aa67c4a320a
“CHEST” Spirometry System
TW: “捷舒特”肺功能測定儀
Taiwan·Risk Class 2·MD·CHEST MIYAGI FACTORY·Registered Mar 14, 2019 – Mar 14, 2024ExpiredRegistration details
- Analysis ID
- dae576848c521f60990c8aa67c4a320a
- License Form
- Ministry of Health Medical Device Import No. 032297
- Customs Code
- DHA05603229704
Company information
- Manufacturer
- CHEST MIYAGI FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- HOM TAH MEDICAL INSTRUMENTS CORPORATION
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 14, 2019
- Expiry Date
- Mar 14, 2024
About this record
Access comprehensive regulatory information for “CHEST” Spirometry System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dae576848c521f60990c8aa67c4a320a and manufactured by CHEST MIYAGI FACTORY. The authorized representative in Taiwan is HOM TAH MEDICAL INSTRUMENTS CORPORATION.
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