Taiwan FDA registration 917859c5bcb5ab8c065b584fc990de05

"ESU" Transilluminator (Non-Sterile)

TW: "醫仕優" 透照器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·ESU LLP·Registered Jun 25, 2015 – Jun 25, 2025Expired
Registration details
Analysis ID
917859c5bcb5ab8c065b584fc990de05
License Form
Ministry of Health Medical Device Import No. 015380
Customs Code
DHA09401538001
Company information
Manufacturer
ESU LLP
Manufacturer Country
Japan
Authorized Representative
J.HEART TECHNOLOGY CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Translucent Apparatus (M.1945)".
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M1945 transillumination
Import Information
Imported from abroad
Dates and status
Registration Date
Jun 25, 2015
Expiry Date
Jun 25, 2025
About this record

Access comprehensive regulatory information for "ESU" Transilluminator (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 917859c5bcb5ab8c065b584fc990de05 and manufactured by ESU LLP. The authorized representative in Taiwan is J.HEART TECHNOLOGY CO., LTD..

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