Pure Global

"弘采" 爬汯戯機 - Taiwan Registration a9e788e2b71b3d358c3e396ebd2dcdad

Access comprehensive regulatory information for "弘采" 爬汯戯機 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a9e788e2b71b3d358c3e396ebd2dcdad and manufactured by THERALIFE INTERVENTION CARE COMPANY LIMITED. The authorized representative in Taiwan is THERALIFE INTERVENTION CARE COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free Database
Powered by Pure Global AI
89,000+ Devices
a9e788e2b71b3d358c3e396ebd2dcdad
Registration Details
Taiwan FDA Registration: a9e788e2b71b3d358c3e396ebd2dcdad
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"弘采" 爬汯戯機
TW: "弘采" 爬梯機
Risk Class 1

Registration Details

a9e788e2b71b3d358c3e396ebd2dcdad

Company Information

Taiwan, Province of China

Product Details

It is limited to the first level of identification of the "Power Patient Conveyor (O.5150)" of the Medical Equipment Classification and Grading Management Measures.

o Physical Medical Sciences

O.5150 5150.

Domestic

Dates and Status

Apr 15, 2015

Apr 15, 2025