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"Skytec" manual patient transport device (unsterilized) - Taiwan Registration 4fad5c8567f80939b52605b7904aa441

Access comprehensive regulatory information for "Skytec" manual patient transport device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4fad5c8567f80939b52605b7904aa441 and manufactured by SKEDCO, INC.. The authorized representative in Taiwan is ADEPT GENERAL CORP..

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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4fad5c8567f80939b52605b7904aa441
Registration Details
Taiwan FDA Registration: 4fad5c8567f80939b52605b7904aa441
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Device Details

"Skytec" manual patient transport device (unsterilized)
TW: "ๆ€ๅ‡ฑๅพ—"ๆ‰‹ๅ‹•็—…ๆ‚ฃ่ผธ้€่ฃ็ฝฎ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

4fad5c8567f80939b52605b7904aa441

DHA04400359704

Company Information

United States

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".

J General hospital and personal use equipment

J.6785 Manual Patient Conveying Device

import

Dates and Status

Apr 12, 2006

Apr 12, 2026

Sep 30, 2021

Cancellation Information

Logged out

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