Taiwan FDA registration a5cfc63b59c5379c2215bd587a2a5798
"Terumo" sar continued intravenous indwelling needle
TW: "泰爾茂"紗爾續靜脈留置針
Taiwan·Risk Class 2·KOFU FACTORY OF TERUMO CORPORATION·Registered Jun 25, 1999 – Feb 09, 2029ActiveRegistration details
- Analysis ID
- a5cfc63b59c5379c2215bd587a2a5798
- Customs Code
- DHA00600921704
Company information
- Manufacturer
- KOFU FACTORY OF TERUMO CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- TERUMO TAIWAN MEDICAL CO., LTD.
Product details
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5200 Endovascular catheters
- Import Information
- import
Dates and status
- Registration Date
- Jun 25, 1999
- Expiry Date
- Feb 09, 2029
About this record
Access comprehensive regulatory information for "Terumo" sar continued intravenous indwelling needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a5cfc63b59c5379c2215bd587a2a5798 and manufactured by KOFU FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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