Taiwan FDA registration e070418a680f2c18a4822759d5498533

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

TW: "屹龍" 交替式壓力氣墊床(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·HILLROM DE MEXICO S DE RL DE CV·Registered Jun 18, 2019 – Jun 18, 2024Expired
Registration details
Analysis ID
e070418a680f2c18a4822759d5498533
License Form
Ministry of Health Medical Device Import No. 020563
Customs Code
DHA09402056303
Company information
Manufacturer Country
Mexico
Authorized Representative
CONPLUS INTERNATIONAL CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Alternating Pressure Air Mattress (J.5550)".
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J5550 Alternating pressure air mattress
Import Information
Imported from abroad
Dates and status
Registration Date
Jun 18, 2019
Expiry Date
Jun 18, 2024
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About this record

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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