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"SAMARIT" Manual Patient Transfer Device (Non-Sterile) - Taiwan Registration f4681a742f7582adf51e71637729463b

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 f4681a742f7582adf51e71637729463b and manufactured by SAMARIT MEDICAL AG. The authorized representative in Taiwan is ROTARY TRADING CO., LTD..

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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f4681a742f7582adf51e71637729463b
Registration Details
Taiwan FDA Registration: f4681a742f7582adf51e71637729463b
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Device Details

"SAMARIT" Manual Patient Transfer Device (Non-Sterile)
TW: "่ŽŽ็‘ช้›ท็‰น" ๆ‰‹ๅ‹•็—…ๆ‚ฃ่ผธ้€่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

f4681a742f7582adf51e71637729463b

Ministry of Health Medical Device Import No. 021185

DHA09402118502

Company Information

Switzerland

Product Details

J General hospital and personal use equipment

J6785 Manual Patient Conveyor

Imported from abroad

Dates and Status

Jan 13, 2020

Jan 13, 2025

Cancellation Information

Logged out

่ฝ‰็‚บ็™ป้Œ„ๅญ—่™Ÿ

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