Taiwan FDA registration 5e4f84010367c2017a1edfaae442fa18
"Ambi" blood bag line rush blood forceps (unsterilized)
TW: "艾盟比" 血袋管路趕血鉗 (未滅菌)
Taiwan·Risk Class 1·LMB TECHNOLOGIE GMBH·Registered May 07, 2010 – May 07, 2020CancelledRegistration details
- Analysis ID
- 5e4f84010367c2017a1edfaae442fa18
- Customs Code
- DHA04400853800
Company information
- Manufacturer
- LMB TECHNOLOGIE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- AMAZING MEDICAL INC.
Product details
- Intended Use
- Squeeze the residual blood from the blood bag line into the blood bag.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9050 Blood bank supply equipment
- Import Information
- import
Dates and status
- Registration Date
- May 07, 2010
- Expiry Date
- May 07, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Ambi" blood bag line 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 5e4f84010367c2017a1edfaae442fa18 and manufactured by LMB TECHNOLOGIE GMBH. The authorized representative in Taiwan is AMAZING MEDICAL INC..
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