Taiwan FDA registration 98aa5c532e0e7eec127f3b6bd62a1697
"TERUMO" REDIFOCUS GLIDECATH
TW: 葛來血管攝影導管
Taiwan·Risk Class 2·MD·ASHITAKA FACTORY OF TERUMO CORPORATION·Registered Feb 14, 1997 – Feb 09, 2029ActiveRegistration details
- Analysis ID
- 98aa5c532e0e7eec127f3b6bd62a1697
- License Form
- Department of Health Medical Device Import No. 008156
- Customs Code
- DHA00600815605
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
- Produced in Taiwan, China
Dates and status
- Registration Date
- Feb 14, 1997
- Expiry Date
- Feb 09, 2029
About this record
Access comprehensive regulatory information for "TERUMO" REDIFOCUS GLIDECATH in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 98aa5c532e0e7eec127f3b6bd62a1697 and manufactured by ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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