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Headlamp for the "Pireody" procedure (unsterilized) - Taiwan Registration 2a73608864687d37671d78549fa6fe05

Access comprehensive regulatory information for Headlamp for the "Pireody" procedure (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2a73608864687d37671d78549fa6fe05 and manufactured by PERIOPTIX INC.. The authorized representative in Taiwan is INTERLINK MEDICAL 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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2a73608864687d37671d78549fa6fe05
Registration Details
Taiwan FDA Registration: 2a73608864687d37671d78549fa6fe05
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Device Details

Headlamp for the "Pireody" procedure (unsterilized)
TW: "ๅ€้Šณๆญๅธ"ๆ‰‹่ก“็”จ้ ญ็‡ˆ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

2a73608864687d37671d78549fa6fe05

DHA04401111304

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

Nov 28, 2011

Nov 28, 2016

Jun 25, 2018

Cancellation Information

Logged out

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