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"Lenet" non-powered treatment mattress (unsterilized) - Taiwan Registration 8c1da723e71fc7c82cbe1262142d6e88

Access comprehensive regulatory information for "Lenet" non-powered treatment 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 8c1da723e71fc7c82cbe1262142d6e88 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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8c1da723e71fc7c82cbe1262142d6e88
Registration Details
Taiwan FDA Registration: 8c1da723e71fc7c82cbe1262142d6e88
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Device Details

"Lenet" non-powered treatment mattress (unsterilized)
TW: โ€œ่Šๅ…ง็‰นโ€ ้žๅ‹•ๅŠ›ๅผๆฒป็™‚ๅบŠๅขŠ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

8c1da723e71fc7c82cbe1262142d6e88

DHA084a0012402

Company Information

Czechia

Product Details

Limited to the first level identification range of the classification and grading management method for medical equipment "Non-powered floating therapy mattress (J.5150)".

J General hospital and personal use equipment

J.5150 Non-powered floating therapy mattress

Dates and Status

Oct 15, 2022

Oct 31, 2025