Taiwan FDA registration 31863ba4b8dbf9dff64c883ae664e48a

“ARJO” Patient Lifting (Non-Sterile)

TW: “洱久”病患移位升降機 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·ARJO INTERNATIONAL AB·Registered Sep 05, 2017 – Sep 05, 2022Expired
Registration details
Analysis ID
31863ba4b8dbf9dff64c883ae664e48a
License Form
Ministry of Health Medical Device Import No. 018272
Customs Code
DHA09401827200
Company information
Manufacturer Country
Canada
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
Sep 05, 2017
Expiry Date
Sep 05, 2022
Companies making similar products

Top companies providing products similar to "“ARJO” Patient Lifting (Non-Sterile)"

Recent registrations

Recently registered similar products

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 31863ba4b8dbf9dff64c883ae664e48a and manufactured by ARJO INTERNATIONAL AB. The authorized representative in Taiwan is TAIWAN PROFESSIONAL MEDICAL TECHNOLOGY INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ARJOHUNTLEIGH POLSKA SP. ZO. O., and 1 recent registrations in the same category. 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 DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations