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"Sebrondo" manual instruments for general surgery (unsterilized) - Taiwan Registration d7ec5f8b5d7cc9f1e144da81f23e67cd

Access comprehensive regulatory information for "Sebrondo" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d7ec5f8b5d7cc9f1e144da81f23e67cd and manufactured by SYBRONENDO. The authorized representative in Taiwan is P & H BIOTECH CORP..

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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d7ec5f8b5d7cc9f1e144da81f23e67cd
Registration Details
Taiwan FDA Registration: d7ec5f8b5d7cc9f1e144da81f23e67cd
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Device Details

"Sebrondo" manual instruments for general surgery (unsterilized)
TW: โ€œๅกžๅธƒๆœ—ๆฉๆœตโ€ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

d7ec5f8b5d7cc9f1e144da81f23e67cd

DHA04401198509

Company Information

United States

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, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

import

Dates and Status

Jul 26, 2012

Jul 26, 2017

Nov 26, 2019

Cancellation Information

Logged out

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