Taiwan FDA registration 2aedfb2189863315721f7c396be1509d

“Schiller” Electrocardiographs

TW: “錫樂”心電圖系統
Taiwan flagTaiwan·Risk Class 2·MD·SCHILLER AG·Registered May 22, 2017 – May 22, 2027Active
Registration details
Analysis ID
2aedfb2189863315721f7c396be1509d
License Form
Ministry of Health Medical Device Import No. 029767
Customs Code
DHA05602976705
Company information
Manufacturer
SCHILLER AG
Manufacturer Country
Switzerland
Authorized Representative
FUTUREMED TECHNOLOGY CORPORATION
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular devices
Product Type (Level 2)
E2340 ECG Scanner
Import Information
Imported from abroad
Dates and status
Registration Date
May 22, 2017
Expiry Date
May 22, 2027
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About this record

Access comprehensive regulatory information for “Schiller” Electrocardiographs in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2aedfb2189863315721f7c396be1509d 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 3 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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