Taiwan FDA registration 3d603e6497a0c2fcde465908cb54d9c0

"Medical Tech" alternating pressure air mattress (unsterilized)

TW: “醫技”交替式壓力氣墊床 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·EEZCARE MEDICAL CORP.·Registered Aug 25, 2011 – Aug 25, 2016Cancelled
Registration details
Analysis ID
3d603e6497a0c2fcde465908cb54d9c0
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
E-GMED HEALTH 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
Aug 25, 2011
Expiry Date
Aug 25, 2016
Cancellation Date
Jun 26, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Medical Tech" 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 3d603e6497a0c2fcde465908cb54d9c0 and manufactured by EEZCARE MEDICAL CORP.. The authorized representative in Taiwan is E-GMED HEALTH 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.

Free DatabasePowered by Pure Global AI89,000+ Devices