Taiwan FDA registration d2c01c4caf20c930e32c399edcd283ad
"Termo" Navoklos supports the catheter
TW: “泰爾茂”納伏克洛斯支持導管
Taiwan·Risk Class 2·TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION·Registered Apr 21, 2017 – Apr 21, 2027ActiveRegistration details
- Analysis ID
- d2c01c4caf20c930e32c399edcd283ad
- Customs Code
- DHA05602967309
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- TERUMO TAIWAN MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Apr 21, 2017
- Expiry Date
- Apr 21, 2027
About this record
Access comprehensive regulatory information for "Termo" Navoklos supports the catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d2c01c4caf20c930e32c399edcd283ad and manufactured by TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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