Taiwan FDA registration 480c2770b618abd138c5db1817dd593b

"Edrite" non-powered treatment mattress (unsterilized)

TW: “愛迪麗特”非動力式治療床墊(未滅菌)
Taiwan flagTaiwan·Risk Class 1·ARTILAT N.V.·Registered Mar 14, 2008 – Mar 14, 2013Cancelled
Registration details
Analysis ID
480c2770b618abd138c5db1817dd593b
Customs Code
DHA04400658308
Company information
Manufacturer
ARTILAT N.V.
Manufacturer Country
Belgium
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Therapeutic Mattresses (J.5150)".
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J.5150 Non-powered floating therapy mattress
Import Information
import
Dates and status
Registration Date
Mar 14, 2008
Expiry Date
Mar 14, 2013
Cancellation Date
Mar 21, 2013
Cancellation information
Status
Logged out
Reason
自請註銷
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About this record

Access comprehensive regulatory information for "Edrite" non-powered treatment 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 480c2770b618abd138c5db1817dd593b and manufactured by ARTILAT N.V.. The authorized representative in Taiwan is EVERCARE MEDICAL INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ARTILAT NV, and 1 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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