Taiwan FDA registration 1d5364ebf1ab9b6562f558c9c1e90f0c

SANKEN AITERNATING PRESSURE AIR FLOTATION MATTRESS (NON-STERILE)

TW: 三研交替式壓力氣墊床(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·SANWA KAKEN KOGYO CO., LTD.·Registered Jun 16, 2015 – Jun 16, 2020Cancelled
Registration details
Analysis ID
1d5364ebf1ab9b6562f558c9c1e90f0c
License Form
Ministry of Health Medical Device Import No. 015349
Customs Code
DHA09401534907
Company information
Manufacturer Country
Japan
Authorized Representative
HURN ARNG ENTERPRISE CO., LTD.
Product details
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
Jun 16, 2015
Expiry Date
Jun 16, 2020
Cancellation Date
Jun 22, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for SANKEN AITERNATING 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 1d5364ebf1ab9b6562f558c9c1e90f0c and manufactured by SANWA KAKEN KOGYO CO., LTD.. The authorized representative in Taiwan is HURN ARNG ENTERPRISE CO., LTD..

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