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“Schiller” Spirometry Devices - Taiwan Registration 7536678bfffd5d931e4140ec42d80b00

Access comprehensive regulatory information for “Schiller” Spirometry Devices in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7536678bfffd5d931e4140ec42d80b00 and manufactured by SCHILLER AG. The authorized representative in Taiwan is FUTUREMED TECHNOLOGY CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SCHILLER AG, 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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7536678bfffd5d931e4140ec42d80b00
Registration Details
Taiwan FDA Registration: 7536678bfffd5d931e4140ec42d80b00
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Device Details

“Schiller” Spirometry Devices
TW: “錫樂”肺量計
Risk Class 2
MD
Cancelled

Registration Details

7536678bfffd5d931e4140ec42d80b00

Ministry of Health Medical Device Import No. 027298

DHA05602729802

Company Information

Switzerland

Product Details

D Devices for anesthesiology

D1840 Spirometer for diagnosis

Imported from abroad

Dates and Status

May 21, 2015

May 21, 2020

May 19, 2022

Cancellation Information

Logged out

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