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"Tontarra" Manual surgical instruments (Non-Sterile) - Taiwan Registration 03b752a5f91d8efd47f658ecef21d9c6

Access comprehensive regulatory information for "Tontarra" Manual surgical instruments (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 03b752a5f91d8efd47f658ecef21d9c6 and manufactured by TONTARRA MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is SMARTECH MEDICAL CO., LTD..

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03b752a5f91d8efd47f658ecef21d9c6
Registration Details
Taiwan FDA Registration: 03b752a5f91d8efd47f658ecef21d9c6
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Device Details

"Tontarra" Manual surgical instruments (Non-Sterile)
TW: "้€š็‰นๆ‹‰" ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

03b752a5f91d8efd47f658ecef21d9c6

Ministry of Health Medical Device Import No. 018475

DHA09401847501

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

Nov 07, 2017

Nov 07, 2022