Taiwan FDA registration e4cb2de56fbc026ce7c2a2c25380c882
"Emma" diode laser
TW: “愛瑪”二極體雷射
Registration details
- Analysis ID
- e4cb2de56fbc026ce7c2a2c25380c882
- Customs Code
- DHA00602256402
Company information
- Manufacturer
- Alma Lasers GmbH;; Alma Lasers Ltd.
- Manufacturer Country
- Israel;;Germany
- Authorized Representative
- NEOASIA LTD.
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.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- import
Dates and status
- Registration Date
- Jun 24, 2011
- Expiry Date
- Jun 24, 2026
About this record
Access comprehensive regulatory information for "Emma" diode laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e4cb2de56fbc026ce7c2a2c25380c882 and manufactured by Alma Lasers GmbH;; Alma Lasers Ltd.. The authorized representative in Taiwan is NEOASIA LTD..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices