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“Aesculap”Rigid laryngoscope (Non-sterile) - Taiwan Registration 6c7c6cc0d460dcfc1ee9bfec2b51a3d5

Access comprehensive regulatory information for “Aesculap”Rigid laryngoscope (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6c7c6cc0d460dcfc1ee9bfec2b51a3d5 and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..

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6c7c6cc0d460dcfc1ee9bfec2b51a3d5
Registration Details
Taiwan FDA Registration: 6c7c6cc0d460dcfc1ee9bfec2b51a3d5
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Device Details

“Aesculap”Rigid laryngoscope (Non-sterile)
TW: “雅氏”硬式喉頭鏡 (未滅菌)
Risk Class 1
MD

Registration Details

6c7c6cc0d460dcfc1ee9bfec2b51a3d5

Ministry of Health Medical Device Import No. 021684

DHA09402168407

Company Information

Germany

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Rigid Laryngoscopy (D.5540)".

D Devices for anesthesiology

D5540 Rigid laryngoscope

Imported from abroad

Dates and Status

Jul 01, 2020

Jul 01, 2025