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"Akrus" Manual Patient Transfer Device (Non-Sterile) - Taiwan Registration d97aeb7fee9dc554cf0b9d79b18a53f6

Access comprehensive regulatory information for "Akrus" Manual Patient Transfer Device (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 d97aeb7fee9dc554cf0b9d79b18a53f6 and manufactured by AKRUS GMBH & CO. KG. The authorized representative in Taiwan is SUMTAGE ENTERPRISE CO., LTD..

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d97aeb7fee9dc554cf0b9d79b18a53f6
Registration Details
Taiwan FDA Registration: d97aeb7fee9dc554cf0b9d79b18a53f6
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Device Details

"Akrus" Manual Patient Transfer Device (Non-Sterile)
TW: "้›…ๅ…‹้ญฏๆ–ฏ" ๆ‰‹ๅ‹•็—…ๆ‚ฃ่ผธ้€่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d97aeb7fee9dc554cf0b9d79b18a53f6

Ministry of Health Medical Device Import No. 016713

DHA09401671307

Company Information

Germany

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".

J General hospital and personal use equipment

J6785 Manual Patient Conveyor

Imported from abroad

Dates and Status

Jun 27, 2016

Jun 27, 2021