Taiwan FDA registration 4c1f6eb60759c4cf1d39910c6ca104af

Airbi Blood Mixer and Blood Gravimetric Analysis Device (Unsterilized)

TW: “艾爾畢”倍美血液混合器及血液重量分析裝置 (未滅菌)

Taiwan·Risk Class 1·LMB Technologie GmbH·Registered Oct 01, 2021 – Oct 31, 2024Expired

Registration details

Analysis ID: 4c1f6eb60759c4cf1d39910c6ca104af
Customs Code: DHA08402053400

Company information

Manufacturer: LMB Technologie GmbH
Manufacturer Country: Germany
Authorized Representative: AMAZING MEDICAL INC.

Product details

Intended Use: It is limited to the first level of identification of the "Blood Mixer and Blood Gravimetric Analysis Device (B.9195)" of the Administrative Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.9195 Blood Mixers and Blood Gravimetric Analysis Devices
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Oct 01, 2021
Expiry Date: Oct 31, 2024

About this record

Access comprehensive regulatory information for Airbi Blood Mixer and Blood Gravimetric Analysis Device (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4c1f6eb60759c4cf1d39910c6ca104af and manufactured by LMB Technologie GmbH. The authorized representative in Taiwan is AMAZING MEDICAL INC..

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