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“APEX”PRESSURE RELIEF PAD (Non-Sterile) - Taiwan Registration 334fc5dcee19cdc78f3bb664e7b87f5a

Access comprehensive regulatory information for “APEX”PRESSURE RELIEF PAD (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 334fc5dcee19cdc78f3bb664e7b87f5a and manufactured by APEX MEDICAL (KUNSHAN) CORP.. The authorized representative in Taiwan is Wellell Inc..

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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334fc5dcee19cdc78f3bb664e7b87f5a
Registration Details
Taiwan FDA Registration: 334fc5dcee19cdc78f3bb664e7b87f5a
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Device Details

“APEX”PRESSURE RELIEF PAD (Non-Sterile)
TW: “雅博”減壓氣墊 (未滅菌)
Risk Class 1
MD

Registration Details

334fc5dcee19cdc78f3bb664e7b87f5a

Department of Health Medical Device Land Transport No. 000338

DHA04600033807

Company Information

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

J5550 Alternating pressure air mattress

Imported from abroad; Made in China

Dates and Status

Jan 19, 2007

Jan 19, 2027