Taiwan FDA registration cc9c12929fd398b7c46a0a03d14ffbda
"Eccleris" surgical headlamp (unsterilized)
TW: "艾克萊里斯"手術用頭燈(未滅菌)
Registration details
- Analysis ID
- cc9c12929fd398b7c46a0a03d14ffbda
- Customs Code
- DHA09401456100
Company information
- Manufacturer
- EUSA GLOBAL LLC;; ECLERIS USA
- Manufacturer Country
- United States
- Authorized Representative
- BOYANG MEDICAL TECHNOLOGY CO., LTD
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Surgical Headlamp (M.4335)" first level identification range.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4335 Headlamps for surgery
- Import Information
- import
Dates and status
- Registration Date
- Oct 13, 2014
- Expiry Date
- Oct 13, 2029
About this record
Access comprehensive regulatory information for "Eccleris" surgical headlamp (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cc9c12929fd398b7c46a0a03d14ffbda and manufactured by EUSA GLOBAL LLC;; ECLERIS USA. The authorized representative in Taiwan is BOYANG MEDICAL TECHNOLOGY CO., 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