Taiwan FDA registration 12b3c7d0bd916eb72fb4b664dad9016d

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

TW: "輔滅拭" 手動式眼科手術器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·RUMEX INTERNATIONAL COMPANY·Registered Oct 14, 2016 – Oct 14, 2021Expired
Registration details
Analysis ID
12b3c7d0bd916eb72fb4b664dad9016d
License Form
Ministry of Health Medical Device Import No. 017083
Customs Code
DHA09401708305
Company information
Manufacturer Country
United States
Authorized Representative
MEDBEST ENTERPRISE 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
Oct 14, 2016
Expiry Date
Oct 14, 2021
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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 12b3c7d0bd916eb72fb4b664dad9016d and manufactured by RUMEX INTERNATIONAL COMPANY. The authorized representative in Taiwan is MEDBEST ENTERPRISE 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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