Taiwan FDA registration a85757209253c11905cfcd69b8d81528
“COMDEK” Sleep Apnea Analysis System
TW: “康定”睡眠呼吸分析系統
Taiwan·Risk Class 2·MD·COMDEK INDUSTRIAL CORPORATION·Registered Jul 05, 2016 – Jul 05, 2026ExpiredRegistration details
- Analysis ID
- a85757209253c11905cfcd69b8d81528
- License Form
- Ministry of Health Medical Device Manufacturing No. 005410
Company information
- Manufacturer
- COMDEK INDUSTRIAL CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- COMDEK INDUSTRIAL 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)
- D2377 Aborted Breath Monitor
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jul 05, 2016
- Expiry Date
- Jul 05, 2026
About this record
Access comprehensive regulatory information for “COMDEK” Sleep Apnea Analysis System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a85757209253c11905cfcd69b8d81528 and manufactured by COMDEK INDUSTRIAL CORPORATION. The authorized representative in Taiwan is COMDEK INDUSTRIAL CORPORATION.
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