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"Ruidato" powered airflow floating treatment bed - Taiwan Registration 092cb16ca7fdba0a62496fc26c2aab5e

Access comprehensive regulatory information for "Ruidato" powered airflow floating treatment bed in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 092cb16ca7fdba0a62496fc26c2aab5e and manufactured by REDACTRON INTERNATIONAL B.V.. The authorized representative in Taiwan is MEDITECHS 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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092cb16ca7fdba0a62496fc26c2aab5e
Registration Details
Taiwan FDA Registration: 092cb16ca7fdba0a62496fc26c2aab5e
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Device Details

"Ruidato" powered airflow floating treatment bed
TW: "็‘ž้”้€š"ๅ‹•ๅŠ›ๅผๆฐฃๆต้ฃ„ๆตฎๆฒป็™‚ๅบŠ
Risk Class 1
Cancelled

Registration Details

092cb16ca7fdba0a62496fc26c2aab5e

DHA04400238408

Company Information

Netherlands

Product Details

It treats bedsores, burns and helps blood circulation.

o Physical Medical Sciences

O.5170 5170.

import

Dates and Status

Dec 28, 2005

Dec 28, 2010

Apr 30, 2014

Cancellation Information

Logged out

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