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"Rumex" Manual ophthalmic surgical instrument (Sterile) - Taiwan Registration 92397856bb0667f4765a6b31d09894d3

Access comprehensive regulatory information for "Rumex" Manual ophthalmic surgical instrument (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 92397856bb0667f4765a6b31d09894d3 and manufactured by RUMEX INTERNATIONAL LTD. The authorized representative in Taiwan is BIOMEGA INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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92397856bb0667f4765a6b31d09894d3
Registration Details
Taiwan FDA Registration: 92397856bb0667f4765a6b31d09894d3
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Device Details

"Rumex" Manual ophthalmic surgical instrument (Sterile)
TW: "็พ…็พŽๆ€" ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆป…่Œ)
Risk Class 1
MD

Registration Details

92397856bb0667f4765a6b31d09894d3

Ministry of Health Medical Device Import No. 020746

DHA09402074601

Company Information

United Kingdom

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".

M Ophthalmic devices

M4350 Manual Ophthalmic Surgery Instrument

Imported from abroad

Dates and Status

Aug 13, 2019

Aug 13, 2024