Taiwan FDA registration 6a1173f5f17207020e3011c7fe98dda0
"Gebeike" with valve tear guide
TW: “葛貝可”帶閥撕裂式導引器
Taiwan·Risk Class 2·GREATBATCH MEDICAL INC·Registered Dec 17, 2012 – Dec 17, 2017CancelledRegistration details
- Analysis ID
- 6a1173f5f17207020e3011c7fe98dda0
- Customs Code
- DHA00602426005
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
- Dec 17, 2012
- Expiry Date
- Dec 17, 2017
- Cancellation Date
- Nov 26, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Gebeike" with valve tear guide in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6a1173f5f17207020e3011c7fe98dda0 and manufactured by GREATBATCH MEDICAL INC. The authorized representative in Taiwan is LORION ENTERPRISES INC..
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