Taiwan FDA registration bab9028b6e116293149ddd460828f3ad
RADIFOCUS GUIDE WIRE M "TERUMO"
TW: 導引導線
Taiwan·Risk Class 2·MD·ASHITAKA FACTORY OF TERUMO CORPORATION·Registered Sep 08, 1997 – Feb 09, 2029ActiveRegistration details
- Analysis ID
- bab9028b6e116293149ddd460828f3ad
- License Form
- Department of Health Medical Device Import No. 008394
- Customs Code
- DHA00600839408
Company information
- Manufacturer
- ASHITAKA FACTORY OF TERUMO CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- TERUMO TAIWAN MEDICAL CO., LTD.
Product details
- Product Type (Level 1)
- 0600 Intensive care unit and cardiac intensive monitoring
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 08, 1997
- Expiry Date
- Feb 09, 2029
About this record
Access comprehensive regulatory information for RADIFOCUS GUIDE WIRE M "TERUMO" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bab9028b6e116293149ddd460828f3ad and manufactured by ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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