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"Ellard" limb equipment (unsterilized) - Taiwan Registration e4a23c0c6cfa382b7835163c358021fa

Access comprehensive regulatory information for "Ellard" limb equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e4a23c0c6cfa382b7835163c358021fa and manufactured by ALLARD USA INC.. The authorized representative in Taiwan is CHENG CHUAN P&O 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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e4a23c0c6cfa382b7835163c358021fa
Registration Details
Taiwan FDA Registration: e4a23c0c6cfa382b7835163c358021fa
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Device Details

"Ellard" limb equipment (unsterilized)
TW: "่‰พๆ‹‰ๅพท" ่‚ข้ซ”่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

e4a23c0c6cfa382b7835163c358021fa

DHA08401374601

Company Information

United States

Product Details

Limited to the first level recognition range of medical equipment classification and grading management measures limb equipment (O.3475).

o Physical Medical Sciences

O.3475 Limb fittings

import

Dates and Status

Oct 01, 2021

Oct 31, 2025