Taiwan FDA registration d2bb718f63d136f2ed9205828048f0e8
“Skytron” AURORA 4 LED Surgical Lights
TW: “司凱壯”色溫可調發光二極體手術燈
Taiwan·Risk Class 2·MD·Dai-Ichi Shomei Co., Ltd.·Registered Jan 16, 2018 – Jan 16, 2028ActiveRegistration details
- Analysis ID
- d2bb718f63d136f2ed9205828048f0e8
- License Form
- Ministry of Health Medical Device Import No. 030689
- Customs Code
- DHA05603068901
Company information
- Manufacturer
- Dai-Ichi Shomei Co., Ltd.
- Manufacturer Country
- Japan
- Authorized Representative
- SYM-MED ENTERPRISE CO., LTD
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4580 Surgical light
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 16, 2018
- Expiry Date
- Jan 16, 2028
About this record
Access comprehensive regulatory information for “Skytron” AURORA 4 LED Surgical Lights in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d2bb718f63d136f2ed9205828048f0e8 and manufactured by Dai-Ichi Shomei Co., Ltd.. The authorized representative in Taiwan is SYM-MED ENTERPRISE CO., LTD.
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