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“Strengthen”Manual patient transfer device (Non-Sterile)  - Taiwan Registration 9c2c5513d714532b4f4be808533c69ef

Access comprehensive regulatory information for “Strengthen”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 9c2c5513d714532b4f4be808533c69ef and manufactured by ALLIANCE MANUFACTURING SERVICE, INC.. The authorized representative in Taiwan is Johnson & Johnson Medical Devices, Inc.

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9c2c5513d714532b4f4be808533c69ef
Registration Details
Taiwan FDA Registration: 9c2c5513d714532b4f4be808533c69ef
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Device Details

“Strengthen”Manual patient transfer device (Non-Sterile) 
TW: “強生”手動病患輸送裝置 (未滅菌)
Risk Class 1
MD

Registration Details

9c2c5513d714532b4f4be808533c69ef

Ministry of Health Medical Device Import Registration No. 012202

DHA08401220205

Company Information

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

Oct 01, 2021

Oct 31, 2023