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"Immedia" Manual patient transfer device (Non-Sterile) - Taiwan Registration 79f72fab04cc9bd47a0e7ed16dee6de4

Access comprehensive regulatory information for "Immedia" 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 79f72fab04cc9bd47a0e7ed16dee6de4 and manufactured by ETAC AB, REG. 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.

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79f72fab04cc9bd47a0e7ed16dee6de4
Registration Details
Taiwan FDA Registration: 79f72fab04cc9bd47a0e7ed16dee6de4
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Device Details

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

Registration Details

79f72fab04cc9bd47a0e7ed16dee6de4

Ministry of Health Medical Device Import No. 019986

DHA09401998605

Company Information

Sweden

Product Details

J General hospital and personal use equipment

J6785 Manual Patient Conveyor

Imported from abroad

Dates and Status

Jan 02, 2019

Jan 02, 2024

Cancellation Information

Logged out

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