Taiwan FDA registration c6dce22f5d881fc6b6484b1691dd108a
"Pioneer" Euro 3 LED surgical light
TW: “史開創”歐羅3 LED外科手術燈
Taiwan·Risk Class 2·Skytron, LLC.; Dai-Ichi Shomei Co., Ltd.·Registered Mar 05, 2014 – Mar 05, 2019CancelledRegistration details
- Analysis ID
- c6dce22f5d881fc6b6484b1691dd108a
- Customs Code
- DHA05602596604
Company information
- Manufacturer
- Skytron, LLC.; Dai-Ichi Shomei Co., Ltd.
- Manufacturer Country
- United States;;Japan
- Authorized Representative
- MEDIGIANT ENTERPRISE CO., 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.4580 Surgical lamp
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Mar 05, 2014
- Expiry Date
- Mar 05, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Pioneer" Euro 3 LED surgical light in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c6dce22f5d881fc6b6484b1691dd108a and manufactured by Skytron, LLC.; Dai-Ichi Shomei Co., Ltd.. The authorized representative in Taiwan is MEDIGIANT ENTERPRISE CO., LTD..
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