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“STERIS” HarmonyAIR A-Series Surgical Lighting System - Taiwan Registration 4bd5c38cea97be58052f715f248fdf97

Access comprehensive regulatory information for “STERIS” HarmonyAIR A-Series 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 4bd5c38cea97be58052f715f248fdf97 and manufactured by STERIS CORPORATION. The authorized representative in Taiwan is MEDTRUST INTERNATIONAL 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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4bd5c38cea97be58052f715f248fdf97
Registration Details
Taiwan FDA Registration: 4bd5c38cea97be58052f715f248fdf97
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Device Details

“STERIS” HarmonyAIR A-Series Surgical Lighting System
TW: “思泰瑞”哈莫寧艾爾A系列手術燈系統
Risk Class 2
MD

Registration Details

4bd5c38cea97be58052f715f248fdf97

Ministry of Health Medical Device Import No. 035573

DHA05603557304

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4580 Surgical light

Imported from abroad

Dates and Status

Jun 10, 2022

Jun 10, 2027