Taiwan FDA registration 73a401c1408ad1913248e76663537b77

“DERMACARE” Intense Pulsed Light System

TW: “德瑪凱”脈衝光系統
Taiwan flagTaiwan·Risk Class 2·MD·Demacai Co., Ltd. Nanke Branch·Registered Nov 05, 2013 – Nov 05, 2018Cancelled
Registration details
Analysis ID
73a401c1408ad1913248e76663537b77
License Form
Ministry of Health Medical Device Manufacturing No. 004232
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
DERMACARE BIOMED INC.
Product details
Product Type (Level 1)
I General and plastic surgical devices
Product Type (Level 2)
I4810 Lasers for general surgery, plastic surgery and dermatology
Import Information
Produced in Taiwan, China
Dates and status
Registration Date
Nov 05, 2013
Expiry Date
Nov 05, 2018
Cancellation Date
May 19, 2022
Cancellation information
Status
Logged out
Reason
許可證逾有效期未申請展延
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About this record

Access comprehensive regulatory information for “DERMACARE” Intense Pulsed Light System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 73a401c1408ad1913248e76663537b77 and manufactured by Demacai Co., Ltd. Nanke Branch. The authorized representative in Taiwan is DERMACARE BIOMED INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DERMACARE BIOMED INC., and 1 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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