Taiwan FDA registration da4c345421c1062816ffb28bbc8d7b8a

"RUMEX" Manual Ophthalmic Surgical Instruments (Non-Sterile)

TW: "滷美斯"手動式眼科手術器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·RUMEX INTERNATIONAL COMPANY·Registered Dec 22, 2020 – Dec 22, 2025Expired
Registration details
Analysis ID
da4c345421c1062816ffb28bbc8d7b8a
License Form
Ministry of Health Medical Device Import No. 022192
Customs Code
DHA09402219204
Company information
Manufacturer Country
United States
Authorized Representative
EVERLIGHT INSTRUMENT CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".
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
Dec 22, 2020
Expiry Date
Dec 22, 2025
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About this record

Access comprehensive regulatory information for "RUMEX" Manual Ophthalmic Surgical Instruments (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 da4c345421c1062816ffb28bbc8d7b8a and manufactured by RUMEX INTERNATIONAL COMPANY. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RUMEX INTERNATIONAL COMPANY, and 2 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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