Taiwan FDA registration 0e6e636214f468044a2aabfe5a42ce8a
"Armambi" electric blood bag pipe rush blood forceps (unsterilized)
TW: “艾盟比”電動血袋管路趕血鉗（未滅菌）
Taiwan·Risk Class 1·LMB TECHNOLOGIE GMBH·Registered Jun 28, 2010 – Jun 28, 2015CancelledRegistration details
- Analysis ID
- 0e6e636214f468044a2aabfe5a42ce8a
- Customs Code
- DHA04400894602
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
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jun 28, 2010
- Expiry Date
- Jun 28, 2015
- Cancellation Date
- Aug 09, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Armambi" electric 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 0e6e636214f468044a2aabfe5a42ce8a and manufactured by LMB TECHNOLOGIE GMBH. The authorized representative in Taiwan is AMAZING MEDICAL INC..
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