Identity
- Trade Name
- Vyntus FDA UDI
- Generic Name
- Electrocardiography telemetric monitoring system transmitter FDA UDI
- Device Name
- Vyntus ECG FDA UDI
- Model / Reference
- V-707356 FDA UDI
- Description
- Vyntus ECG FDA UDI
Identifiers
- Catalog Number
- V-707356 FDA UDI
- Primary DI / UDI-DI
- 34250892904970 FDA UDI
- 510(k) Number
- K150810 FDA UDI
- FDA Product Code
- BZC FDA UDI
- GMDN Term
- Electrocardiography telemetric monitoring system transmitter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.1880 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Electrocardiography telemetric monitoring system transmitter
Vyntus by Vyaire Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K150810 also covers:
- Vyaire — Jaeger Medical GmbH
- Vyaire — Jaeger Medical GmbH
- Vyaire — Jaeger Medical GmbH
- Vyaire — Jaeger Medical GmbH
- Vyaire — Jaeger Medical GmbH
- Vyaire — Jaeger Medical GmbH
- Vyaire — Jaeger Medical GmbH
- Vyaire — Jaeger Medical GmbH
- Vyaire — Jaeger Medical GmbH
- Vyaire — Jaeger Medical GmbH
- Vyaire — Jaeger Medical GmbH
- Vyaire — Jaeger Medical GmbH
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
- Vyaire Medical, Inc.
Sources (1)
- FDA UDI 494aedbc-fa68-4fff-85d2-6e2791a1f6bd 36 fields · synced May 30, 2026