Taiwan FDA registration 9ffb8edc3042105b134b8be8703d5ce3
SURFLASH "TERUMO"
TW: 紗爾續靜脈留置針
Taiwan·Risk Class 2·MD·KOFU FACTORY OF TERUMO CORPORATION·Registered Jun 25, 1999 – Feb 09, 2029ActiveRegistration details
- Analysis ID
- 9ffb8edc3042105b134b8be8703d5ce3
- License Form
- Department of Health Medical Device Import No. 009217
- 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)
- 1399 Other blood transfusion, infusion equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 25, 1999
- Expiry Date
- Feb 09, 2029
About this record
Access comprehensive regulatory information for SURFLASH "TERUMO" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9ffb8edc3042105b134b8be8703d5ce3 and manufactured by KOFU FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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