Uni-Patch
- Primary DI
- 90884521167847
- Brand
- Uni-Patch
- Company
- Cardinal Health, Inc.
- Model
- EC89455
- Catalog number
- EC89455
- Device description
- Specialty Stimulating Electrodes,699
- Published
- 2016-09-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Contact Domains#
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 |
|---|---|---|---|---|
| 90884521167847 | Package | GS1 | 400 | In Commercial Distribution |
| 10884521167841 | Primary | GS1 | 0 | |
| 10884521537033 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 90884521167847 | 90884521167847 |
| 10884521167841 | 10884521167841 |
| 10884521537033 | 10884521537033 |
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 | 1.75 | Inch |
| Width | 1.75 | Inch |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | ; |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(508)261-8000 | covidien.udi@covidien.com |
Regulatory Flags#
- DUNS number
- 080935429
- Device count
- 40
- 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
- false
- 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 |
|---|---|---|---|---|
| 10884521015920 | Dover | 20512C | 20512C | 2016-09-24 |
| 10884521015982 | Dover | 20520C | 20520C | 2016-09-24 |
| 10884521016002 | Dover | 20522C | 20522C | 2016-10-13 |
| 10884521024991 | Kendall | 9240 | 9240 | 2018-06-27 |
| 10884521025004 | Kendall | 9242 | 9242 | 2018-06-27 |
| 10884521025011 | Kendall | 9243 | 9243 | 2018-06-27 |
| 10884521025028 | Kendall | 9244 | 9244 | 2018-06-27 |
| 20192253002062 | Curity | 2146 | 2146- | 2018-12-12 |
| 20884521143064 | Magellan | 8881833515 | 8881833515 | 2016-09-24 |
| 10884527007110 | Argyle | 8888163055 | 8888163055 | 2016-09-24 |
| 10885380173691 | Curity | 6309G | 6309G | 2019-11-14 |
| 20885380173544 | Curity | 9022G | 9022G | 2019-11-14 |
| 20885380173568 | Curity | 9024G | 9024G | 2019-11-14 |
| 10884521141148 | Filac | 504083 | 504083 | 2016-09-24 |
| 10884521165045 | Kangaroo | 388106 | 388106 | 2016-09-24 |
| 10884521000674 | Dover | 3531 | 3531- | 2016-09-24 |
| 10884521001046 | Dover | 6255 | 6255 | 2016-09-24 |
| 10884521001138 | Dover | 8256 | 8256 | 2016-09-24 |
| 10884521001145 | Dover | 701672 | 701672 | 2016-09-24 |
| 10884521001206 | Dover | 7004ICLL | 7004ICLL | 2016-09-24 |
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