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"Lenette" alternating pressure air mattress (unsterilized) - Taiwan Registration 1d20747c5ad2388167efe8560fef0d49

Access comprehensive regulatory information for "Lenette" alternating pressure air mattress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1d20747c5ad2388167efe8560fef0d49 and manufactured by LINET SPOL. S R. O.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.

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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1d20747c5ad2388167efe8560fef0d49
Registration Details
Taiwan FDA Registration: 1d20747c5ad2388167efe8560fef0d49
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Device Details

"Lenette" alternating pressure air mattress (unsterilized)
TW: "่Šๅ…ง็‰น" ไบคๆ›ฟๅผๅฃ“ๅŠ›ๆฐฃๅขŠๅบŠ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

1d20747c5ad2388167efe8560fef0d49

DHA09402301207

Company Information

Czechia

Product Details

Limited to the classification and grading management method of medical equipment "Alternating pressure air mattress (J.5550)" level identification range.

J General hospital and personal use equipment

J.5550 ไบคๆ›ฟๅผๅฃ“ๅŠ›ๆฐฃๅขŠๅบŠ

Input;; QMS/QSD

Dates and Status

Jan 12, 2023

Jan 12, 2028