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"CONDOR" Manual Surgical Instrument for General Use (Non-sterile) - Taiwan Registration 2c2421c0d7b58c0a6520cc98389234ee

Access comprehensive regulatory information for "CONDOR" 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 2c2421c0d7b58c0a6520cc98389234ee and manufactured by CONDOR MedTec GmbH. The authorized representative in Taiwan is EVOLUTION WORLDWIDE 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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2c2421c0d7b58c0a6520cc98389234ee
Registration Details
Taiwan FDA Registration: 2c2421c0d7b58c0a6520cc98389234ee
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Device Details

"CONDOR" Manual Surgical Instrument for General Use (Non-sterile)
TW: "ๅบทๆœต" ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2c2421c0d7b58c0a6520cc98389234ee

Ministry of Health Medical Device Import No. 020247

DHA09402024706

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

Mar 28, 2019

Mar 28, 2024