Taiwan FDA registration 18ce972373893714b1055997eb0b1df8

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

TW: "熠隆" 交替式壓力氣墊床 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·HILL-ROM DE MEXICO S DE RL DE CV·Registered Jul 16, 2020 – Jul 16, 2025Expired
Registration details
Analysis ID
18ce972373893714b1055997eb0b1df8
License Form
Ministry of Health Medical Device Import No. 021749
Customs Code
DHA09402174909
Company information
Manufacturer Country
Mexico
Authorized Representative
Hill-Rom Taiwan 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
Jul 16, 2020
Expiry Date
Jul 16, 2025
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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 18ce972373893714b1055997eb0b1df8 and manufactured by HILL-ROM DE MEXICO S DE RL DE CV. The authorized representative in Taiwan is Hill-Rom Taiwan Ltd..

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including HILL-ROM, INC., HILLROM DE MEXICO S DE RL DE CV, 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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