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"GUENTER BISSINGER" Manual surgical instrument for general use (Non-Sterile) - Taiwan Registration 1a17e47ddaf25787e669f5015cad4790

Access comprehensive regulatory information for "GUENTER BISSINGER" 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 1a17e47ddaf25787e669f5015cad4790 and manufactured by GUENTER BISSINGER MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is SMARTECH MEDICAL CO., LTD..

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1a17e47ddaf25787e669f5015cad4790
Registration Details
Taiwan FDA Registration: 1a17e47ddaf25787e669f5015cad4790
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Device Details

"GUENTER BISSINGER" Manual surgical instrument for general use (Non-Sterile)
TW: "ๅ›็‰นๆฏ”่พ›ๆ ผ" ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

1a17e47ddaf25787e669f5015cad4790

Ministry of Health Medical Device Import No. 016426

DHA09401642604

Company Information

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 21, 2016

Apr 21, 2021