“DERMACARE” Intense Pulsed Light System
Taiwan·Risk Class 2·MD·DERMACARE BIOMED INC.·Registered Jan 08, 2019 – Jan 08, 2024Cancelled- Analysis ID
- 83e4b1d71d8dbdeace0e82076ff05db8
- License Form
- Ministry of Health Medical Device Manufacturing No. 006311
- Manufacturer
- DERMACARE BIOMED INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DERMACARE BIOMED INC.
- 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
- Registration Date
- Jan 08, 2019
- Expiry Date
- Jan 08, 2024
- Cancellation Date
- Jan 04, 2023
- Status
- Logged out
- Reason
- 自請註銷
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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 83e4b1d71d8dbdeace0e82076ff05db8 and manufactured by DERMACARE BIOMED INC.. The authorized representative in Taiwan is DERMACARE BIOMED INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Demacai Co., Ltd. Nanke Branch, 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.