Taiwan FDA registration ccb6bde36c5f6f073b879ddcf6fbd1e4
“Skytron” AURORA ASTRO LED Surgical Lights
TW: “司凱壯”艾斯特羅發光二極體手術燈
Taiwan·Risk Class 2·MD·Dai-Ichi Shomei Co., Ltd.·Registered Apr 02, 2019 – Apr 02, 2024ExpiredRegistration details
- Analysis ID
- ccb6bde36c5f6f073b879ddcf6fbd1e4
- License Form
- Ministry of Health Medical Device Import No. 032362
- Customs Code
- DHA05603236202
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
- Apr 02, 2019
- Expiry Date
- Apr 02, 2024
About this record
Access comprehensive regulatory information for “Skytron” AURORA ASTRO 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 ccb6bde36c5f6f073b879ddcf6fbd1e4 and manufactured by Dai-Ichi Shomei Co., Ltd.. The authorized representative in Taiwan is SYM-MED ENTERPRISE CO., LTD.
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