Taiwan FDA registration 04172491834a5a05c86041f38b921bfd

"Wacoal" in vitro prosthesis (unsterilized)

TW: “華歌爾”體外用義乳(未滅菌)
Taiwan flagTaiwan·Risk Class 1·WACOAL CORP.·Registered Nov 27, 2012 – Nov 27, 2022Cancelled
Registration details
Analysis ID
04172491834a5a05c86041f38b921bfd
Customs Code
DHA04401241805
Company information
Manufacturer
WACOAL CORP.
Manufacturer Country
Japan
Authorized Representative
TAIWAN WACOAL CO., LTD.
Product details
Intended Use
Limited to the first level recognition range of medical equipment management measures for in vitro cosmetic repair supplements (I.3800).
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.3800 Repair supplement for cosmetic use in the body
Import Information
import
Dates and status
Registration Date
Nov 27, 2012
Expiry Date
Nov 27, 2022
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "Wacoal" in vitro prosthesis (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 04172491834a5a05c86041f38b921bfd and manufactured by WACOAL CORP.. The authorized representative in Taiwan is TAIWAN WACOAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TRULIFE, and 2 recent registrations in the same category. 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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