Taiwan FDA registration e588ad38f77dab53691aa6600391a525

"Mitsubishi" medical ultrasound image output paper (unsterilized)

TW: “三菱”醫療超音波影像輸出用紙 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MITSUBISHI ELECTRIC CORPORATION·Registered May 05, 2006 – May 05, 2011Cancelled
Registration details
Analysis ID
e588ad38f77dab53691aa6600391a525
Customs Code
DHA04400438000
Company information
Manufacturer Country
Japan
Authorized Representative
PAI LEA ENT. CO., LTD.
Product details
Intended Use
It is limited to the scope of the first level of identification of the "Paper Recorder (E.2810)" of the Administrative Measures for Medical Devices. Paper used to record physiological amplifiers, signal conditioners or computer signals is not used for measurement purposes.
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.2810 紙張式記錄器
Import Information
import
Dates and status
Registration Date
May 05, 2006
Expiry Date
May 05, 2011
Cancellation Date
Nov 30, 2012
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Mitsubishi" medical ultrasound image output paper (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e588ad38f77dab53691aa6600391a525 and manufactured by MITSUBISHI ELECTRIC CORPORATION. The authorized representative in Taiwan is PAI LEA ENT. CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MITSUBISHI ELECTRIC CORPORATION, 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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