Taiwan FDA registration 4beafc11b208876954e545cda2426f7b
"Anpo" physiological monitoring equipment
TW: “安睿”生理監視設備
Taiwan·Risk Class 2·Iradimed Corporation·Registered Apr 10, 2018 – Apr 10, 2023ExpiredRegistration details
- Analysis ID
- 4beafc11b208876954e545cda2426f7b
- Customs Code
- DHA05603080105
Company information
- Manufacturer
- Iradimed Corporation
- Manufacturer Country
- United States
- Authorized Representative
- GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology; E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.2300 心臟監視器(包含心動數計和心率警示器);; E.2700 血氧飽和測定儀;; D.1700 氧化亞氮(笑氣)分析儀
- Import Information
- import
Dates and status
- Registration Date
- Apr 10, 2018
- Expiry Date
- Apr 10, 2023
About this record
Access comprehensive regulatory information for "Anpo" physiological monitoring equipment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4beafc11b208876954e545cda2426f7b and manufactured by Iradimed Corporation. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.
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