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“STERIS” HarmonyAIR Surgical Lighting System - Taiwan Registration 1fc57ded385a50cb138aad8a6d086adf

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 1fc57ded385a50cb138aad8a6d086adf and manufactured by STERIS CORPORATION. The authorized representative in Taiwan is HSIN TUNG MEDICAL 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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1fc57ded385a50cb138aad8a6d086adf
Registration Details
Taiwan FDA Registration: 1fc57ded385a50cb138aad8a6d086adf
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Device Details

“STERIS” HarmonyAIR Surgical Lighting System
TW: “斯泰瑞”哈莫尼艾手術燈
Risk Class 2
MD

Registration Details

1fc57ded385a50cb138aad8a6d086adf

Ministry of Health Medical Device Import No. 030653

DHA05603065303

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

Dec 19, 2017

Dec 19, 2022

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