Taiwan FDA registration 899cde83bc07936aad0ba000090caa97

"Rifton" Non-AC-powered patient lift (Non-Sterile)

TW: "立動"非交流電力式病患升降機(未滅菌)

Taiwan·Risk Class 1·MD·COMMUNITY PRODUCTS, LLC DOING BUSINESS AS RIFTON EQUIPMENT·Registered Jul 18, 2018 – Jul 18, 2023Expired

Registration details

Analysis ID: 899cde83bc07936aad0ba000090caa97
License Form: Ministry of Health Medical Device Import No. 019321
Customs Code: DHA09401932105

Company information

Manufacturer: COMMUNITY PRODUCTS, LLC DOING BUSINESS AS RIFTON EQUIPMENT
Manufacturer Country: United States
Authorized Representative: ABILITIES HEALTHCARE INCORPORATED

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: Jul 18, 2018
Expiry Date: Jul 18, 2023

About this record

Access comprehensive regulatory information for "Rifton" Non-AC-powered patient lift (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 899cde83bc07936aad0ba000090caa97 and manufactured by COMMUNITY PRODUCTS, LLC DOING BUSINESS AS RIFTON EQUIPMENT. The authorized representative in Taiwan is ABILITIES HEALTHCARE INCORPORATED.

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