Taiwan FDA registration b0c3ac5e0e51d8146c6e2179498b1ec5

"Home" alternating pressure air mattress (unsterilized)

TW: "居家"交替式壓力氣墊床(未滅菌)

Taiwan·Risk Class 1·EEZCARE MEDICAL CORP.·Registered Feb 23, 2011 – Feb 23, 2021Cancelled

Registration details

Analysis ID: b0c3ac5e0e51d8146c6e2179498b1ec5

Company information

Manufacturer: EEZCARE MEDICAL CORP.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: TAIWAN HEALTH CARE 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): J.5550 交替式壓力氣墊床
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Feb 23, 2011
Expiry Date: Feb 23, 2021
Cancellation Date: Oct 12, 2023

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Home" alternating pressure air mattress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b0c3ac5e0e51d8146c6e2179498b1ec5 and manufactured by EEZCARE MEDICAL CORP.. The authorized representative in Taiwan is TAIWAN HEALTH CARE 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.