Taiwan FDA registration 6383fbdfefb2d87f7a99d7c08a673f17

"Gilder" Cool Leveling System

TW: “吉爾得”酷思塑平系統
Taiwan flagTaiwan·Risk Class 2·ZELTIQ AESTHETICS, INC.·Registered Jan 29, 2018 – Jan 29, 2023Cancelled
Registration details
Analysis ID
6383fbdfefb2d87f7a99d7c08a673f17
Customs Code
DHA05603069302
Company information
Manufacturer Country
United States
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4340 Contact Cooling Units
Import Information
The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input
Dates and status
Registration Date
Jan 29, 2018
Expiry Date
Jan 29, 2023
Cancellation Date
Jun 12, 2023
Cancellation information
Status
Logged out
Reason
自請註銷
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About this record

Access comprehensive regulatory information for "Gilder" Cool Leveling System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6383fbdfefb2d87f7a99d7c08a673f17 and manufactured by ZELTIQ AESTHETICS, INC.. The authorized representative in Taiwan is ALLERGAN PHARMACEUTICALS TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ZELTIQ AESTHETICS, INC., 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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