Taiwan FDA registration c608b8fadd1a3204f313f6c40b80791e
"Arnuoxon" condensed RF incision probe set
TW: “愛諾生”冷凝射頻切口探針組
Registration details
- Analysis ID
- c608b8fadd1a3204f313f6c40b80791e
- Customs Code
- DHA05602947709
Company information
- Manufacturer
- Advent S. de R.L. de C.V.;; Avanos Medical, Inc.
- Manufacturer Country
- Mexico;;United States
- Authorized Representative
- BUTICON INTERNATIONAL CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.4400 Shot Cutout Generator
- Import Information
- import
Dates and status
- Registration Date
- Mar 07, 2017
- Expiry Date
- Mar 07, 2027
About this record
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.
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