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“CHEST” Multifunctional Spirometer - Taiwan Registration f2905d87c4de7b0befd198898fe99e65

Access comprehensive regulatory information for “CHEST” Multifunctional Spirometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f2905d87c4de7b0befd198898fe99e65 and manufactured by CHEST MIYAGI FACTORY. The authorized representative in Taiwan is HOM TAH MEDICAL INSTRUMENTS CORPORATION.

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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f2905d87c4de7b0befd198898fe99e65
Registration Details
Taiwan FDA Registration: f2905d87c4de7b0befd198898fe99e65
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Device Details

“CHEST” Multifunctional Spirometer
TW: “捷舒特”肺機能測定儀
Risk Class 2
MD

Registration Details

f2905d87c4de7b0befd198898fe99e65

Ministry of Health Medical Device Import No. 027286

DHA05602728605

Company Information

Japan

Product Details

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

D Devices for anesthesiology

D1840 Spirometer for diagnosis

Imported from abroad

Dates and Status

May 06, 2015

May 06, 2025