Taiwan FDA registration 728466d92f6d4d79cd38b992eb46c955
"Gebeike" peelable introduction tube kit
TW: “葛貝可”可剝式導入管工具組
Taiwan·Risk Class 2·GREATBATCH MEDICAL INC·Registered Oct 03, 2011 – Oct 03, 2021CancelledRegistration details
- Analysis ID
- 728466d92f6d4d79cd38b992eb46c955
- Customs Code
- DHA00602283405
Company information
- Manufacturer
- GREATBATCH MEDICAL INC
- Manufacturer Country
- United States
- Authorized Representative
- LORION ENTERPRISES INC.
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.1340 Catheter Introducers
- Import Information
- import
Dates and status
- Registration Date
- Oct 03, 2011
- Expiry Date
- Oct 03, 2021
- Cancellation Date
- Oct 12, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Gebeike" peelable introduction tube kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 728466d92f6d4d79cd38b992eb46c955 and manufactured by GREATBATCH MEDICAL INC. The authorized representative in Taiwan is LORION ENTERPRISES INC..
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