Identity
- Trade Name
- Midmark IQecg® Digital ECG FDA UDI
- Generic Name
- Electrocardiograph, professional, multichannel FDA UDI
- Device Name
- The IQecg®from Midmark is an easy-to-use, digital, 12-lead resting ECG solution that helps you quickly administer testing and access patient information you need to make informed cardiac assessments and provide more efficient patient care. FDA UDI
- Model / Reference
- 1-100-1325 FDA UDI
- Description
- The IQecg®from Midmark is an easy-to-use, digital, 12-lead resting ECG solution that helps you quickly administer testing and access patient information you need to make informed cardiac assessments and provide more efficient patient care. FDA UDI
Identifiers
- Catalog Number
- 1-100-1325 FDA UDI
- Primary DI / UDI-DI
- 00841709100901 FDA UDI
- FDA Product Code
- DPS FDA UDI
- GMDN Term
- Electrocardiograph, professional, multichannel FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2340 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
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Lot / Batch Number
No
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Serial Number
Yes
FDA UDI
Expiration Date
No
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Manufacturing Date
Yes
FDA UDI
Category: Electrocardiograph, professional, multichannel
Midmark IQecg® Digital ECG by Midmark Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Midmark Corporation
Sources (1)
- FDA UDI 69932ec3-6ccb-4761-b863-dafe9a28fdae 37 fields · synced Jun 8, 2026