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"APEXCARE" Manual patient transfer device (Non-Sterile) - Taiwan Registration d7b04351f97d0318bd403dae823c93a6

Access comprehensive regulatory information for "APEXCARE" 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 d7b04351f97d0318bd403dae823c93a6 and manufactured by APEX HEALTH CARE MFG., INC.. The authorized representative in Taiwan is APEX HEALTH CARE MFG., INC..

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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d7b04351f97d0318bd403dae823c93a6
Registration Details
Taiwan FDA Registration: d7b04351f97d0318bd403dae823c93a6
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Device Details

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

Registration Details

d7b04351f97d0318bd403dae823c93a6

Ministry of Health Medical Device Manufacturing No. 007100

Company Information

Taiwan, Province of China

Product Details

J General hospital and personal use equipment

J6785 Manual Patient Conveyor

Produced in Taiwan, China

Dates and Status

Jan 31, 2018

Jan 31, 2023

Cancellation Information

Logged out

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