Taiwan FDA registration cc2ee2014e7fde8406a5ab2ee82ac0fd
"Pioneer" Nordillos surgical light
TW: “史開創”諾帝樂司外科手術燈
Taiwan·Risk Class 2·Skytron, LLC;;DAI-ICHI SHOMEI CO. LTD·Registered Dec 03, 2013 – Dec 03, 2018CancelledRegistration details
- Analysis ID
- cc2ee2014e7fde8406a5ab2ee82ac0fd
- Customs Code
- DHA05602562109
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
- Contract manufacturing;; input
Dates and status
- Registration Date
- Dec 03, 2013
- Expiry Date
- Dec 03, 2018
- 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" Nordillos 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 cc2ee2014e7fde8406a5ab2ee82ac0fd and manufactured by Skytron, LLC;;DAI-ICHI SHOMEI CO. LTD. The authorized representative in Taiwan is MEDIGIANT ENTERPRISE CO., LTD..
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