Identity
- Trade Name
- CareFusion FDA UDI
- Generic Name
- Electrocardiographic electrode, single-use FDA UDI
- Device Name
- ELECTRODE, ADULT, FOAM, ROUND, WET GEL, 50/POUCH FDA UDI
- Model / Reference
- 2009110-050W FDA UDI
- Description
- ELECTRODE, ADULT, FOAM, ROUND, WET GEL, 50/POUCH FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08809083941550 FDA UDI
- 510(k) Number
- K083148 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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Electrocardiographic electrode, single-use
CareFusion by Bioprotech Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Electrocardiographic electrode, single-use.
- ECG leadwire — Shenzhen City Teveik Technology Co., Ltd. · Class I
- Elektrody EKG — SORIMEX sp. z o.o. · Class I
- ECG — Zoll Medical Corporation · Class II
- SWAROMED — TYROLMED GmbH · Class II
- SWAROMED — TYROLMED GmbH · Class II
- SWAROMED — TYROLMED GmbH · Class II
- PG10S /RU26 — FIAB S.p.A. · Class I
- Medline — MEDLINE INDUSTRIES, INC. · Class II
Cleared under the same submission
K083148 also covers:
- Vyaire — Airlife, Inc.
- Baxter — BIOPROTECH INC.
- MediMax Tech — MEDIMAX TECH INC.
- MediMax Tech — MEDIMAX TECH INC.
- MediMax Tech — MEDIMAX TECH INC.
- MediMax Tech — MEDIMAX TECH INC.
- MediMax Tech — MEDIMAX TECH INC.
- MediMax Tech — MEDIMAX TECH INC.
- MediMax Tech — MEDIMAX TECH INC.
- MediMax Tech — MEDIMAX TECH INC.
- MediMax Tech — MEDIMAX TECH INC.
- MediMax Tech — MEDIMAX TECH 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bioprotech Inc.
Sources (1)
- FDA UDI 03365600-f100-46bf-a49a-e87ddd4c2483 36 fields · synced May 30, 2026