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“STERIS” HarmonyAIR Surgical Lighting System - Taiwan Registration c320c7f9d343258c4f7b86dc9a1427b6

Access comprehensive regulatory information for “STERIS” HarmonyAIR Surgical Lighting System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c320c7f9d343258c4f7b86dc9a1427b6 and manufactured by STERIS CORPORATION. The authorized representative in Taiwan is MEDTRUST INTERNATIONAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including STERIS CORPORATION, and 1 recent registrations in the same category. 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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c320c7f9d343258c4f7b86dc9a1427b6
Registration Details
Taiwan FDA Registration: c320c7f9d343258c4f7b86dc9a1427b6
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Device Details

“STERIS” HarmonyAIR Surgical Lighting System
TW: “思泰瑞”哈莫寧艾爾手術燈系統
Risk Class 2
MD

Registration Details

c320c7f9d343258c4f7b86dc9a1427b6

Ministry of Health Medical Device Import No. 032693

DHA05603269302

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

I General and plastic surgical devices

I4580 Surgical light

Imported from abroad

Dates and Status

Jun 22, 2019

Jun 22, 2024

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