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"AR" Manual surgical instrument for general use (Non-Sterile) - Taiwan Registration 582a01851bcabf88d4c499c6f62f3255

Access comprehensive regulatory information for "AR" Manual surgical instrument for general use (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 582a01851bcabf88d4c499c6f62f3255 and manufactured by AUGUST REUCHLEN GMBH. The authorized representative in Taiwan is PRIMA SURGICAL COMPANY.

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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582a01851bcabf88d4c499c6f62f3255
Registration Details
Taiwan FDA Registration: 582a01851bcabf88d4c499c6f62f3255
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Device Details

"AR" Manual surgical instrument for general use (Non-Sterile)
TW: "่‰พ่€ณ" ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

582a01851bcabf88d4c499c6f62f3255

Ministry of Health Medical Device Import No. 015146

DHA09401514606

Company Information

Germany

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Apr 22, 2015

Apr 22, 2025