Taiwan FDA registration f589f62faad191204aa98457cc1e09ca

"ARJO" Patient Lifting (Non-Sterile)

TW: "洱久" 病患移位升降機 (未滅菌)

Taiwan·Risk Class 1·MD·ARJOHUNTLEIGH POLSKA SP. ZO. O.·Registered Apr 15, 2019 – Apr 15, 2024Expired

Registration details

Analysis ID: f589f62faad191204aa98457cc1e09ca
License Form: Ministry of Health Medical Device Import No. 020311
Customs Code: DHA09402031102

Company information

Manufacturer: ARJOHUNTLEIGH POLSKA SP. ZO. O.
Manufacturer Country: Poland
Authorized Representative: TAIWAN PROFESSIONAL MEDICAL TECHNOLOGY INC.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Non-AC Electric Patient Lift (J.5510)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J5510 Non-AC Electric Patient Lift
Import Information: Imported from abroad

Dates and status

Registration Date: Apr 15, 2019
Expiry Date: Apr 15, 2024

About this record

Access comprehensive regulatory information for "ARJO" Patient Lifting (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 f589f62faad191204aa98457cc1e09ca and manufactured by ARJOHUNTLEIGH POLSKA SP. ZO. O.. The authorized representative in Taiwan is TAIWAN PROFESSIONAL MEDICAL TECHNOLOGY INC..

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