Taiwan FDA registration 817b2886b9a4bcba3e15b09d8c2ff097

"Sanwa" double-layer high-performance air mattress (unsterilized)

TW: 〝三和〞雙層高機能氣墊床(未滅菌)
Taiwan flagTaiwan·Risk Class 1·SANWA JAWS KOGYO CO., LTD.·Registered Apr 30, 2012 – Apr 30, 2017Cancelled
Registration details
Analysis ID
817b2886b9a4bcba3e15b09d8c2ff097
Customs Code
DHA04401164501
Company information
Manufacturer Country
Japan
Authorized Representative
MEDFIRST HEALTHCARE SERVICES, INC.
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
import
Dates and status
Registration Date
Apr 30, 2012
Expiry Date
Apr 30, 2017
Cancellation Date
Dec 13, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Sanwa" double-layer high-performance 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 817b2886b9a4bcba3e15b09d8c2ff097 and manufactured by SANWA JAWS KOGYO CO., LTD.. The authorized representative in Taiwan is MEDFIRST HEALTHCARE SERVICES, INC..

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