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"SAMARIT" Manual patient transfer device (Non-Sterile) - Taiwan Registration c1bbc5b39a6b20db7e2748d3d881a71d

Access comprehensive regulatory information for "SAMARIT" 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 c1bbc5b39a6b20db7e2748d3d881a71d and manufactured by SAMARIT MEDICAL AG. The authorized representative in Taiwan is NAN KAI CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SAMARIT MEDICAL AG, and 2 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.

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c1bbc5b39a6b20db7e2748d3d881a71d
Registration Details
Taiwan FDA Registration: c1bbc5b39a6b20db7e2748d3d881a71d
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Device Details

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

Registration Details

c1bbc5b39a6b20db7e2748d3d881a71d

Ministry of Health Medical Device Import No. 019312

DHA09401931204

Company Information

Switzerland

Product Details

J General hospital and personal use equipment

J6785 Manual Patient Conveyor

Imported from abroad

Dates and Status

Jul 17, 2018

Jul 17, 2023

Cancellation Information

Logged out

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