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"Herriken" Manual Eye Surgery Instruments (Sterilization) - Taiwan Registration 5f8634a2d0210d52ed6f9736932e27bf

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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5f8634a2d0210d52ed6f9736932e27bf
Registration Details
Taiwan FDA Registration: 5f8634a2d0210d52ed6f9736932e27bf
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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

5f8634a2d0210d52ed6f9736932e27bf

DHA09401384002

Company Information

United States

Product Details

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.

M Ophthalmology

M.4350 ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Feb 10, 2014

Feb 10, 2024

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