Taiwan FDA registration 9108c57a78c5a0c2e5ca64297885c529

Pyrament Manual Patient Handling Equipment (Unsterilized)

TW: “派樂蒙”手動病患輸送裝置 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·PARAMOUNT BED CO., LTD.·Registered Oct 01, 2009 – Oct 01, 2014Cancelled
Registration details
Analysis ID
9108c57a78c5a0c2e5ca64297885c529
Customs Code
DHA04400816602
Company information
Manufacturer Country
Japan
Authorized Representative
BENQ MEDICAL TECHNOLOGY CORPORATION
Product details
Intended Use
Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J.6785 Manual Patient Conveying Device
Import Information
import
Dates and status
Registration Date
Oct 01, 2009
Expiry Date
Oct 01, 2014
Cancellation Date
May 28, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for Pyrament Manual Patient Handling Equipment (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9108c57a78c5a0c2e5ca64297885c529 and manufactured by PARAMOUNT BED CO., LTD.. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.

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