Taiwan FDA registration 7536678bfffd5d931e4140ec42d80b00

“Schiller” Spirometry Devices

TW: “錫樂”肺量計
Taiwan flagTaiwan·Risk Class 2·MD·SCHILLER AG·Registered May 21, 2015 – May 21, 2020Cancelled
Registration details
Analysis ID
7536678bfffd5d931e4140ec42d80b00
License Form
Ministry of Health Medical Device Import No. 027298
Customs Code
DHA05602729802
Company information
Manufacturer
SCHILLER AG
Manufacturer Country
Switzerland
Authorized Representative
FUTUREMED TECHNOLOGY CORPORATION
Product details
Product Type (Level 1)
D Devices for anesthesiology
Product Type (Level 2)
D1840 Spirometer for diagnosis
Import Information
Imported from abroad
Dates and status
Registration Date
May 21, 2015
Expiry Date
May 21, 2020
Cancellation Date
May 19, 2022
Cancellation information
Status
Logged out
Reason
許可證逾有效期未申請展延
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About this record

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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