Uni-Patch
- Primary DI
- 10884527021932
- Brand
- Uni-Patch
- Company
- Cardinal Health, Inc.
- Model
- EP84580
- Catalog number
- EP84580
- Device description
- True content to be populated as part of rebranding
- Published
- 2016-09-24
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Product Codes#
| Code | Name |
|---|---|
| GXY | ELECTRODE, CUTANEOUS |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| GXY | Electrode, Cutaneous | Neurology | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 90884527021938 | Package | GS1 | 10 | Not in Commercial Distribution |
| 10884527021932 | Primary | GS1 | 0 | |
| 10884521537316 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 90884527021938 | 90884527021938 |
| 10884527021932 | 10884527021932 |
| 10884521537316 | 10884521537316 |
GMDN Terms#
| Term | Definition |
|---|---|
| Transcutaneous electrical stimulation electrode, single-use | An electrical conductor intended to be attached to a patient's skin (noninvasive) to provide therapeutic electrical stimuli through the body surface [e.g., transcutaneous electrical nerve stimulation (TENS), electrical muscle stimulation (EMS), cranial electrotherapy stimulation (CES)]. It is typically a flat, flexible, conductive pad with an adhesive (e.g., gel), or a preformed shape/mechanism designed for attachment to a particular body part (e.g., earclip), connected to a conductive wire. This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Length | 0 | |
| Width | 0 |
Regulatory Flags#
- DUNS number
- 080935429
- Device count
- 2
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10884521000308 | Dover | 2004 | 2004- | 2016-09-24 |
| 10884521000681 | Dover | 2020 | 2020 | 2016-09-24 |
| 10884521001039 | Dover | 2014 | 2014- | 2016-09-24 |
| 10884521001053 | Dover | 2018 | 2018- | 2016-09-24 |
| 10884521001084 | Dover | 6256 | 6256 | 2016-09-24 |
| 10884521009455 | Dover | 3420 | 3420- | 2016-09-24 |
| 10884521009585 | Dover | 3450LF | 3450LF | 2016-09-24 |
| 10884521082403 | Curity | 2600 | 2600 | 2018-06-29 |
| 10884521084216 | Kerlix | 26719 | 26719 | 2018-06-29 |
| 10884521158863 | Kendall | 2419CD | 2419CD | 2018-06-28 |
| 10884527020782 | Curity | 2601 | 2601 | 2018-06-29 |
| 10884521174917 | Devon | 31141206 | 31141206 | 2016-09-24 |
| 10884527009954 | Kendall | 30781747 | 30781747 | 2018-06-23 |
| 10884521015791 | Dover | 8887623125 | 8887623125 | 2016-09-24 |
| 30884527004847 | Kendall | ES82417 | ES82417- | 2016-09-24 |
| 20884521152134 | Covidien | 31145744 | 31145744- | 2016-09-24 |
| 30884521024841 | Kendall | 9236 | 9236 | 2018-06-30 |
| 10884521138247 | Devon | 31146891 | 31146891 | 2016-09-24 |
| 10884521138261 | Devon | 31146893 | 31146893 | 2016-09-24 |
| 10884521154094 | Devon | 31146894 | 31146894 | 2016-09-24 |
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| 08720791374440 | Neuroguard | Technomed Engineering B.V. | GXY | 2024-05-22 |
| 08720791374457 | Neuroguard | Technomed Engineering B.V. | GXY | 2024-05-22 |
| 08720791374471 | Neuroguard | Technomed Engineering B.V. | GXY | 2024-05-22 |
| 08720791374495 | Neuroguard | Technomed Engineering B.V. | GXY | 2024-05-22 |
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