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"Newbis" treatment table (unsterilized) - Taiwan Registration dfaeb23a55f84679cb902dd2c0cd157e

Access comprehensive regulatory information for "Newbis" treatment table (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dfaeb23a55f84679cb902dd2c0cd157e and manufactured by AIRFUN D.O.O.. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS 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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dfaeb23a55f84679cb902dd2c0cd157e
Registration Details
Taiwan FDA Registration: dfaeb23a55f84679cb902dd2c0cd157e
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Device Details

"Newbis" treatment table (unsterilized)
TW: "็ดๆฏ”ๆ–ฏ"ๆฒป็™‚ๆชฏ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

dfaeb23a55f84679cb902dd2c0cd157e

DHA08402048704

Company Information

Slovenia

Product Details

Limited to the first level identification range of the "Treatment Table (O.3520)" of the Measures for the Classification and Grading Management of Medical Equipment.

o Physical Medical Sciences

O.3520 Therapeutic cage

import

Dates and Status

Oct 01, 2021

Oct 31, 2025