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"Renfei" suture knotting instrument (unsterilized) - Taiwan Registration 894a84d8480758ec28d5157bf998c888

Access comprehensive regulatory information for "Renfei" suture knotting instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 894a84d8480758ec28d5157bf998c888 and manufactured by RANFAC CORP.. The authorized representative in Taiwan is MEDLIANCE LTD..

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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894a84d8480758ec28d5157bf998c888
Registration Details
Taiwan FDA Registration: 894a84d8480758ec28d5157bf998c888
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Device Details

"Renfei" suture knotting instrument (unsterilized)
TW: โ€œไปๆ–โ€็ธซ็ทšๆ‰“็ตๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

894a84d8480758ec28d5157bf998c888

DHA04400827102

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

Nov 05, 2009

Nov 05, 2014

Apr 25, 2018

Cancellation Information

Logged out

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