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"Eccleris" surgical headlamp (unsterilized) - Taiwan Registration cc9c12929fd398b7c46a0a03d14ffbda

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.

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cc9c12929fd398b7c46a0a03d14ffbda
Registration Details
Taiwan FDA Registration: cc9c12929fd398b7c46a0a03d14ffbda
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Device Details

"Eccleris" surgical headlamp (unsterilized)
TW: "่‰พๅ…‹่Š้‡Œๆ–ฏ"ๆ‰‹่ก“็”จ้ ญ็‡ˆ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

cc9c12929fd398b7c46a0a03d14ffbda

DHA09401456100

Company Information

United States

Product Details

Limited to the classification and grading management measures of medical equipment "Surgical Headlamp (M.4335)" first level identification range.

M Ophthalmology

M.4335 Headlamps for surgery

import

Dates and Status

Oct 13, 2014

Oct 13, 2029