Taiwan FDA registration 9f1f67fd9ef844c039f44f2e41cca4d0
Gonafen injection needle
TW: 果納芬注射針
Taiwan·Risk Class 2·TERUMO EUROPE N.V.·Registered Oct 14, 2005 – Oct 14, 2015CancelledRegistration details
- Analysis ID
- 9f1f67fd9ef844c039f44f2e41cca4d0
- Customs Code
- DHA00601270208
Company information
- Manufacturer
- TERUMO EUROPE N.V.
- Manufacturer Country
- Belgium
- Authorized Representative
- MERCK LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Import Information
- import
Dates and status
- Registration Date
- Oct 14, 2005
- Expiry Date
- Oct 14, 2015
- Cancellation Date
- Apr 13, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Gonafen injection needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9f1f67fd9ef844c039f44f2e41cca4d0 and manufactured by TERUMO EUROPE N.V.. The authorized representative in Taiwan is MERCK LTD..
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