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"Handicare" Manual patient transfer device (Non-Sterile) - Taiwan Registration 5beefd143cc285e31a4e3033418e67b0

Access comprehensive regulatory information for "Handicare" Manual patient transfer device (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 5beefd143cc285e31a4e3033418e67b0 and manufactured by HANDICARE AB. The authorized representative in Taiwan is OTTO BOCK ASIA PACIFIC LIMITED TAIWAN BRANCH (H.K.).

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.

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5beefd143cc285e31a4e3033418e67b0
Registration Details
Taiwan FDA Registration: 5beefd143cc285e31a4e3033418e67b0
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Device Details

"Handicare" Manual patient transfer device (Non-Sterile)
TW: "ๆผข่ฟชๅก็ˆพ" ๆ‰‹ๅ‹•็—…ๆ‚ฃ่ผธ้€่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

5beefd143cc285e31a4e3033418e67b0

Ministry of Health Medical Device Import No. 020015

DHA09402001501

Company Information

Sweden

Product Details

J General hospital and personal use equipment

J6785 Manual Patient Conveyor

Imported from abroad

Dates and Status

Jan 10, 2019

Jan 10, 2024

Cancellation Information

Logged out

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