Taiwan FDA registration 012bc31932153d59e7edbe307004d8a4
“Fuji” AP-GRIPFLOW Circulation Perfusion Catheter
TW: “富士”主動脈循環灌注導管
Taiwan·Risk Class 2·MD·Fuji Systems Corporation, Shirakawa Plant·Registered Apr 20, 2020 – Apr 20, 2025ExpiredRegistration details
- Analysis ID
- 012bc31932153d59e7edbe307004d8a4
- License Form
- Ministry of Health Medical Device Import No. 033568
- Customs Code
- DHA05603356801
Company information
- Manufacturer
- Fuji Systems Corporation, Shirakawa Plant
- Manufacturer Country
- Japan
- Authorized Representative
- YOO-HOO Limited
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E4210 Vascular catheters, cannula and tubes for cardiopulmonary vascular bypass
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 20, 2020
- Expiry Date
- Apr 20, 2025
About this record
Access comprehensive regulatory information for “Fuji” AP-GRIPFLOW Circulation Perfusion Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 012bc31932153d59e7edbe307004d8a4 and manufactured by Fuji Systems Corporation, Shirakawa Plant. The authorized representative in Taiwan is YOO-HOO Limited.
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