Taiwan FDA registration d1fda81ee2340b5e8ab8c15f066cebd3
"Kawasumi" blood bag pipe rush blood forceps (unsterilized)
TW: "川澄" 血袋管路趕血鉗 (未滅菌)
Taiwan·Risk Class 1·LMB TECHNOLOGIE GMBH·Registered Aug 04, 2016 – Aug 04, 2021CancelledRegistration details
- Analysis ID
- d1fda81ee2340b5e8ab8c15f066cebd3
- Customs Code
- DHA09401686300
Company information
- Manufacturer
- LMB TECHNOLOGIE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- K2 INTERNATIONAL MEDICAL INC.
Product details
- Intended Use
- Squeeze the residual blood from the blood bag line into the bag.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9999 Miscellaneous
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Aug 04, 2016
- Expiry Date
- Aug 04, 2021
- Cancellation Date
- Sep 19, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Kawasumi" blood bag pipe rush blood forceps (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d1fda81ee2340b5e8ab8c15f066cebd3 and manufactured by LMB TECHNOLOGIE GMBH. The authorized representative in Taiwan is K2 INTERNATIONAL MEDICAL INC..
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