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"Navak" alternating pressure air mattress (unsterilized) - Taiwan Registration 549c092d88afecd3ed6919261668a356

Access comprehensive regulatory information for "Navak" 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 549c092d88afecd3ed6919261668a356 and manufactured by NOVACARE GMBH. The authorized representative in Taiwan is SEQUOIA-TWN HEALTHCARE 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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549c092d88afecd3ed6919261668a356
Registration Details
Taiwan FDA Registration: 549c092d88afecd3ed6919261668a356
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Device Details

"Navak" alternating pressure air mattress (unsterilized)
TW: โ€œๅจœ็“ฆๅ…‹โ€ไบคๆ›ฟๅผๅฃ“ๅŠ›ๆฐฃๅขŠๅบŠ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

549c092d88afecd3ed6919261668a356

DHA04401295403

Company Information

Germany

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Alternating Pressure Air Mattress (J.5550)".

J General hospital and personal use equipment

J.5550 ไบคๆ›ฟๅผๅฃ“ๅŠ›ๆฐฃๅขŠๅบŠ

import

Dates and Status

Apr 30, 2013

Apr 30, 2018

Nov 28, 2019

Cancellation Information

Logged out

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