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"Herriken" Manual Eye Surgery Instruments (Sterilization) - Taiwan Registration 7567cb67ca75063d2d2350c898228480

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 7567cb67ca75063d2d2350c898228480 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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7567cb67ca75063d2d2350c898228480
Registration Details
Taiwan FDA Registration: 7567cb67ca75063d2d2350c898228480
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Device Details

"Herriken" Manual Eye Surgery Instruments (Sterilization)
TW: "่ณ€็‘ž่‚ฏ" ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆป…่Œ)
Risk Class 1

Registration Details

7567cb67ca75063d2d2350c898228480

DHA09402353309

Company Information

United States

Product Details

It is limited to the first level of identification of the "Manual Ophthalmic Surgical Instruments (M.4350)" of the Administrative Measures for the Classification and Grading of Medical Devices.

M Ophthalmology

M.4350 ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Jul 10, 2024

Jul 10, 2029

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