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"JOSEF HEISS" Manual surgical instrument for general use (Non-Sterile) - Taiwan Registration 8c7e2be9f433d20c9297a75c23b9a63e

Access comprehensive regulatory information for "JOSEF HEISS" 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 8c7e2be9f433d20c9297a75c23b9a63e and manufactured by JOSEF HEISS MEDICAL GMBH. The authorized representative in Taiwan is Liren Equipment Factory Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including JOSEF HEISS MEDICAL GMBH, 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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8c7e2be9f433d20c9297a75c23b9a63e
Registration Details
Taiwan FDA Registration: 8c7e2be9f433d20c9297a75c23b9a63e
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Device Details

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

Registration Details

8c7e2be9f433d20c9297a75c23b9a63e

Ministry of Health Medical Device Import No. 016568

DHA09401656801

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

May 23, 2016

May 23, 2021

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