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"Acolis" surgical headlamp and its accessories (unsterilized) - Taiwan Registration 18e9ca0bb0d73836c01fcf1702ee8af1

Access comprehensive regulatory information for "Acolis" surgical headlamp and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 18e9ca0bb0d73836c01fcf1702ee8af1 and manufactured by ECLERIS USA, INC.. The authorized representative in Taiwan is WISE HORSE ENTERPRISE 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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18e9ca0bb0d73836c01fcf1702ee8af1
Registration Details
Taiwan FDA Registration: 18e9ca0bb0d73836c01fcf1702ee8af1
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Device Details

"Acolis" surgical headlamp and its accessories (unsterilized)
TW: "่‰พๅฏๅŠ›ๆ–ฏ" ๆ‰‹่ก“็”จ้ ญ็‡ˆๅŠๅ…ถ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

18e9ca0bb0d73836c01fcf1702ee8af1

DHA04401227700

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Surgical Headlamps (M.4335)".

M Ophthalmology

M.4335 Headlamps for surgery

import

Dates and Status

Oct 19, 2012

Oct 19, 2022

Apr 12, 2024

Cancellation Information

Logged out

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