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"STRENGTHEN" Nonpowered flotation therapy mattress (Non-Sterile) - Taiwan Registration 8354bc1b6f59c16d82c0cf2fcd000a19

Access comprehensive regulatory information for "STRENGTHEN" Nonpowered flotation therapy mattress (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8354bc1b6f59c16d82c0cf2fcd000a19 and manufactured by LINET SPOL. S R. O.. The authorized representative in Taiwan is Johnson & Johnson Medical Instruments Inc.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LINET SPOL. S R. O., and 1 recent registrations in the same category. 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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8354bc1b6f59c16d82c0cf2fcd000a19
Registration Details
Taiwan FDA Registration: 8354bc1b6f59c16d82c0cf2fcd000a19
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Device Details

"STRENGTHEN" Nonpowered flotation therapy mattress (Non-Sterile)
TW: "้‡Œๅ…ง็‰น"้žๅ‹•ๅŠ›ๅผๆฒป็™‚ๅบŠๅขŠ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

8354bc1b6f59c16d82c0cf2fcd000a19

Ministry of Health Medical Device Import No. 021247

DHA09402124701

Company Information

Czechia

Product Details

J General hospital and personal use equipment

J5150 Non-powered treatment mattress

Imported from abroad

Dates and Status

Feb 11, 2020

Feb 11, 2025

Cancellation Information

Logged out

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