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"Hillrom" Alternating pressure air flotation mattress (Non-Sterile) - Taiwan Registration e070418a680f2c18a4822759d5498533

Access comprehensive regulatory information for "Hillrom" Alternating pressure air flotation 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 e070418a680f2c18a4822759d5498533 and manufactured by HILLROM DE MEXICO S DE RL DE CV. The authorized representative in Taiwan is CONPLUS INTERNATIONAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including HILL-ROM DE MEXICO S DE RL DE CV, HILL-ROM, INC., and 4 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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e070418a680f2c18a4822759d5498533
Registration Details
Taiwan FDA Registration: e070418a680f2c18a4822759d5498533
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Device Details

"Hillrom" Alternating pressure air flotation mattress (Non-Sterile)
TW: "ๅฑน้พ" ไบคๆ›ฟๅผๅฃ“ๅŠ›ๆฐฃๅขŠๅบŠ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

e070418a680f2c18a4822759d5498533

Ministry of Health Medical Device Import No. 020563

DHA09402056303

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

Dates and Status

Jun 18, 2019

Jun 18, 2024