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LifeWatch Mobile Cardiac Telemetry 3-Lead
FDA UDIClass II (US FDA UDI)
by Lifewatch
Identity
- Trade Name
- LifeWatch Mobile Cardiac Telemetry 3-Lead FDA UDI
- Generic Name
- Electrocardiography telemetric monitoring system transmitter FDA UDI
- Device Name
- 3 Lead Continuous ECG Monitor & Arrhythmia Detector (MCT 3L - International) FDA UDI
- Model / Reference
- MCT 3L-International FDA UDI
- Description
- 3 Lead Continuous ECG Monitor & Arrhythmia Detector (MCT 3L - International) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850725007101 FDA UDI
- 510(k) Number
- K143359 FDA UDI
- FDA Product Code
- DXH FDA UDIDSI FDA UDI
- GMDN Term
- Electrocardiography telemetric monitoring system transmitter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2920 FDA UDI870.1025 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
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Electrocardiography telemetric monitoring system transmitter
LifeWatch Mobile Cardiac Telemetry 3-Lead by Lifewatch — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K143359 also covers:
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
- Lifewatch
Sources (1)
- FDA UDI 25ee5eba-2e2b-41a8-8678-bf08ddc44aeb 35 fields · synced May 30, 2026