Taiwan FDA registration 91f8422e917a78dba4df2f2c7f5b4362

Johnson & Johnson Manual Patient Conveyor (Unsterilized)

TW: “強生”手動病患輸送裝置 (未滅菌)

Taiwan·Risk Class 1·ALLIANCE MANUFACTURING SERVICE, INC.·Registered Sep 25, 2012 – Sep 25, 2022Cancelled

Registration details

Analysis ID: 91f8422e917a78dba4df2f2c7f5b4362
Customs Code: DHA04401220208

Company information

Manufacturer: ALLIANCE MANUFACTURING SERVICE, INC.
Manufacturer Country: Hong Kong
Authorized Representative: Johnson & Johnson Medical Instruments Inc

Product details

Intended Use: Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6785 Manual Patient Conveying Device
Import Information: import

Dates and status

Registration Date: Sep 25, 2012
Expiry Date: Sep 25, 2022
Cancellation Date: Sep 30, 2021

Cancellation information

Status: Logged out
Reason: 轉為登錄字號

About this record

Access comprehensive regulatory information for Johnson & Johnson Manual Patient Conveyor (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 91f8422e917a78dba4df2f2c7f5b4362 and manufactured by ALLIANCE MANUFACTURING SERVICE, INC.. The authorized representative in Taiwan is Johnson & Johnson Medical Instruments Inc.

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