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"Dan Kell" non-AC electric patient lift (unsterilized) - Taiwan Registration 8cd0fa52698de9d2936a2059f7c46af4

Access comprehensive regulatory information for "Dan Kell" non-AC electric patient lift (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8cd0fa52698de9d2936a2059f7c46af4 and manufactured by VANCARE INC.. The authorized representative in Taiwan is FAMOUS INSTRUMENT 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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8cd0fa52698de9d2936a2059f7c46af4
Registration Details
Taiwan FDA Registration: 8cd0fa52698de9d2936a2059f7c46af4
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Device Details

"Dan Kell" non-AC electric patient lift (unsterilized)
TW: "ไธนๅ‡ฑ็ˆพ" ้žไบคๆต้›ปๅŠ›ๅผ็—…ๆ‚ฃๅ‡้™ๆฉŸ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

8cd0fa52698de9d2936a2059f7c46af4

DHA04401049908

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Non-AC Electric Patient Lift (J.5510)".

J General hospital and personal use equipment

J.5510 Non-AC electric patient lifts

import

Dates and Status

Jun 23, 2011

Jun 23, 2021

Aug 28, 2023

Cancellation Information

Logged out

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