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"SKADE" manual patient transport device (unsterilized) - Taiwan Registration 00cf06fe83f00615172b67c193f1d871

Access comprehensive regulatory information for "SKADE" 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 00cf06fe83f00615172b67c193f1d871 and manufactured by SKEDCO, INC. The authorized representative in Taiwan is FU SHING MEDICAL CO., LTD..

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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00cf06fe83f00615172b67c193f1d871
Registration Details
Taiwan FDA Registration: 00cf06fe83f00615172b67c193f1d871
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Device Details

"SKADE" manual patient transport device (unsterilized)
TW: โ€œๆ–ฏๅ‡ฑๅพทโ€ๆ‰‹ๅ‹•็—…ๆ‚ฃ่ผธ้€่ฃ็ฝฎ๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1
Cancelled

Registration Details

00cf06fe83f00615172b67c193f1d871

DHA04400912302

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

Aug 23, 2010

Aug 23, 2020

Jun 16, 2022

Cancellation Information

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