Taiwan FDA registration 5f8634a2d0210d52ed6f9736932e27bf

"Herriken" Manual Eye Surgery Instruments (Sterilization)

TW: "賀瑞肯" 手動式眼科手術器械 (滅菌)
Taiwan flagTaiwan·Risk Class 1·HURRICANE MEDICAL·Registered Feb 10, 2014 – Feb 10, 2024Expired
Registration details
Analysis ID
5f8634a2d0210d52ed6f9736932e27bf
Customs Code
DHA09401384002
Company information
Manufacturer
HURRICANE MEDICAL
Manufacturer Country
United States
Authorized Representative
BIOMEGA INSTRUMENT CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the "Manual Ophthalmic Surgical Instruments (M.4350)" of the Measures for the Classification and Grading of Medical Equipment.
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.4350 手動式眼科手術器械
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Feb 10, 2014
Expiry Date
Feb 10, 2024
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About this record

Access comprehensive regulatory information for "Herriken" Manual Eye Surgery Instruments (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5f8634a2d0210d52ed6f9736932e27bf and manufactured by HURRICANE MEDICAL. The authorized representative in Taiwan is BIOMEGA INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HURRICANE MEDICAL, 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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