Taiwan FDA registration c88c55ea883d3ca08825d9a8070a92ee

"RUMEX" Manual ophthalmic surgical instrument (Non-Sterile)

TW: "如美克斯"手動式眼科手術器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·RUMEX International Company·Registered Nov 13, 2014 – Nov 13, 2019Cancelled
Registration details
Analysis ID
c88c55ea883d3ca08825d9a8070a92ee
License Form
Ministry of Health Medical Device Import No. 014651
Customs Code
DHA09401465101
Company information
Manufacturer Country
United States
Product details
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M4350 Manual Ophthalmic Surgery Instrument
Import Information
Imported from abroad
Dates and status
Registration Date
Nov 13, 2014
Expiry Date
Nov 13, 2019
Cancellation Date
May 19, 2022
Cancellation information
Status
Logged out
Reason
許可證逾有效期未申請展延
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About this record

Access comprehensive regulatory information for "RUMEX" Manual ophthalmic surgical instrument (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 c88c55ea883d3ca08825d9a8070a92ee and manufactured by RUMEX International Company. The authorized representative in Taiwan is Kangcheng Biomedical Technology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RUMEX INTERNATIONAL COMPANY, 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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