Taiwan FDA registration 0a20f4e4a53b9efeb7827cb6500f4c6e

“TUFFCARE” Non-AC-powered patient lift(Non-sterile)

TW: “偉克”非交流電力式病患升降機(未滅菌)

Taiwan·Risk Class 1·MD·SHIN-I MEDICAL MANUFACTURING CO., LTD.·Registered Oct 15, 2020 – Oct 15, 2025Expired

Registration details

Analysis ID: 0a20f4e4a53b9efeb7827cb6500f4c6e
License Form: Ministry of Health Medical Device Manufacturing No. 008636

Company information

Manufacturer: SHIN-I MEDICAL MANUFACTURING CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: SHIN-I MEDICAL MANUFACTURING CO., LTD.

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: Produced in Taiwan, China

Dates and status

Registration Date: Oct 15, 2020
Expiry Date: Oct 15, 2025

About this record

Access comprehensive regulatory information for “TUFFCARE” 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 0a20f4e4a53b9efeb7827cb6500f4c6e and manufactured by SHIN-I MEDICAL MANUFACTURING CO., LTD.. The authorized representative in Taiwan is SHIN-I MEDICAL MANUFACTURING CO., LTD..

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