Taiwan FDA registration b45ce90abb327777bbf53fd5a1c210a2
“Medtronic” CELLO balloon guide catheter
TW: “美敦力”協樂球囊導引導管
Taiwan·Risk Class 2·MD·Fuji Systems Corporation, Shirakawa Plant·Registered May 02, 2016 – May 02, 2026ExpiredRegistration details
- Analysis ID
- b45ce90abb327777bbf53fd5a1c210a2
- License Form
- Ministry of Health Medical Device Import No. 028523
- Customs Code
- DHA05602852301
Company information
- Manufacturer
- Fuji Systems Corporation, Shirakawa Plant
- Manufacturer Country
- Japan
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
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)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 02, 2016
- Expiry Date
- May 02, 2026
About this record
Access comprehensive regulatory information for “Medtronic” CELLO balloon guide catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b45ce90abb327777bbf53fd5a1c210a2 and manufactured by Fuji Systems Corporation, Shirakawa Plant. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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