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"Arnuoxon" condensed RF incision probe set - Taiwan Registration c608b8fadd1a3204f313f6c40b80791e

Access comprehensive regulatory information for "Arnuoxon" condensed RF incision probe set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c608b8fadd1a3204f313f6c40b80791e and manufactured by Advent S. de R.L. de C.V.;; Avanos Medical, Inc.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.

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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c608b8fadd1a3204f313f6c40b80791e
Registration Details
Taiwan FDA Registration: c608b8fadd1a3204f313f6c40b80791e
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Device Details

"Arnuoxon" condensed RF incision probe set
TW: โ€œๆ„›่ซพ็”Ÿโ€ๅ†ทๅ‡ๅฐ„้ ปๅˆ‡ๅฃๆŽข้‡็ต„
Risk Class 2

Registration Details

c608b8fadd1a3204f313f6c40b80791e

DHA05602947709

Company Information

Mexico;;United States

Product Details

For details, it is Chinese approved copy of the imitation order

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K.4400 Shot Cutout Generator

import

Dates and Status

Mar 07, 2017

Mar 07, 2027