Taiwan FDA registration 6f49722335a88f52049ff5b2b876001b

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

TW: "顧德們" 非交流電力式病患升降機 (未滅菌)

Taiwan·Risk Class 1·MD·V. GULDMANN A/S·Registered Oct 09, 2013 – Oct 09, 2023Expired

Registration details

Analysis ID: 6f49722335a88f52049ff5b2b876001b
License Form: Ministry of Health Medical Device Import No. 013486
Customs Code: DHA09401348607

Company information

Manufacturer: V. GULDMANN A/S
Manufacturer Country: Denmark
Authorized Representative: EZ-Care Solution 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: Imported from abroad

Dates and status

Registration Date: Oct 09, 2013
Expiry Date: Oct 09, 2023

About this record

Access comprehensive regulatory information for "Guldmann" 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 6f49722335a88f52049ff5b2b876001b and manufactured by V. GULDMANN A/S. The authorized representative in Taiwan is EZ-Care Solution Co., Ltd..

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.