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"JOSEF HEISS" Manual surgical instrument for general use (Non-Sterile) - Taiwan Registration 247967cac6ec113de4539c56307d1ab8

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 247967cac6ec113de4539c56307d1ab8 and manufactured by JOSEF HEISS MEDICAL GMBH. The authorized representative in Taiwan is PRIMA SURGICAL COMPANY.

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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247967cac6ec113de4539c56307d1ab8
Registration Details
Taiwan FDA Registration: 247967cac6ec113de4539c56307d1ab8
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Device Details

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

Registration Details

247967cac6ec113de4539c56307d1ab8

Ministry of Health Medical Device Import No. 017805

DHA09401780504

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 09, 2017

May 09, 2022

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