Taiwan FDA registration 60265c1012235b66d8395448cbdd01b0
"Terumo" guide line
TW: "泰爾茂"導引導線
Taiwan·Risk Class 2·ASHITAKA FACTORY OF TERUMO CORPORATION·Registered Sep 08, 1997 – Feb 09, 2029ActiveRegistration details
- Analysis ID
- 60265c1012235b66d8395448cbdd01b0
- 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)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1330 Catheter Guide Wires
- Import Information
- import
Dates and status
- Registration Date
- Sep 08, 1997
- Expiry Date
- Feb 09, 2029
About this record
Access comprehensive regulatory information for "Terumo" guide line in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 60265c1012235b66d8395448cbdd01b0 and manufactured by ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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