Identity
- Trade Name
- MediMax Tech FDA UDI
- Generic Name
- Electrocardiographic electrode, single-use FDA UDI
- Device Name
- MXF43TC-30 ECG: PE Foam, Universal, Teardrop 43x45mm, Radiolucent, Carbon Snap, ECG Electrode, 30pcs/Pack, 600pcs/Box, 6000pcs/Master Case FDA UDI
- Model / Reference
- MXF43TC-30 ECG FDA UDI
- Description
- MXF43TC-30 ECG: PE Foam, Universal, Teardrop 43x45mm, Radiolucent, Carbon Snap, ECG Electrode, 30pcs/Pack, 600pcs/Box, 6000pcs/Master Case FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817325021302 FDA UDI
- 510(k) Number
- K020003 FDA UDI
- FDA Product Code
- DRX FDA UDI
- GMDN Term
- Electrocardiographic electrode, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2360 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Category: Electrocardiographic electrode, single-use
MediMax Tech by Medimax Tech Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K020003 also covers:
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- Vyaire — Airlife, Inc.
- Vyaire — Airlife, Inc.
- Vyaire — Airlife, Inc.
- Bio Protech — BIO PROTECH USA, INC.
- Bio Protech — BIO PROTECH USA, INC.
- Bio Protech — BIO PROTECH USA, INC.
- Bio Protech — BIO PROTECH USA, INC.
- Bio Protech — BIO PROTECH USA, INC.
- Bio Protech — BIO PROTECH USA, INC.
- Bio Protech — BIO PROTECH USA, INC.
- Bio Protech — BIO PROTECH USA, INC.
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
- Medimax Tech Inc.
Sources (1)
- FDA UDI 8550c69a-220c-4f11-9605-8f199dfada92 35 fields · synced Jun 6, 2026