Identity
- Trade Name
- MediChoice FDA UDI
- Generic Name
- Electrode conductive skin pad, single-use FDA UDI
- Device Name
- Electrode Defibrillation Electrocardiogram Radiolucent Vinyl Laminated Foam Conductive Foil Adhesive Hydrogel Pacing Equal To Phillips Dp2 Amp Dp6 Amp M3713A Adult Not Made With Natural Rubber Latex MediChoice FDA UDI
- Model / Reference
- MC1710H FDA UDI
- Description
- Electrode Defibrillation Electrocardiogram Radiolucent Vinyl Laminated Foam Conductive Foil Adhesive Hydrogel Pacing Equal To Phillips Dp2 Amp Dp6 Amp M3713A Adult Not Made With Natural Rubber Latex MediChoice FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10885632116629 FDA UDI
- FDA Product Code
- MLN FDA UDI
- GMDN Term
- Electrode conductive skin pad, 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: Electrode conductive skin pad, single-use
MediChoice by Owens & Minor Distribution, Inc. — 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
- Owens & Minor Distribution, Inc.
Sources (1)
- FDA UDI ea6fb5b3-4270-476e-84e8-e8e3f7735258 34 fields · synced May 30, 2026