FDA UDI
Not in Commercial Distribution
🇺🇸 United States
Ives EEG Solutions
DI: 00850012681007
·
Model: DCPE-21/B
·
IVES EEG SOLUTIONS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1
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Basic Information
- Brand Name
- Ives EEG Solutions
- Primary DI
- 00850012681007
- Version / Model
- DCPE-21/B
- Company Name
- IVES EEG SOLUTIONS, LLC
- Labeler DUNS
- 015020106
- Distribution Status
- Not in Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2019-10-29
- Public Version
- 4
- Public Version Date
- 2026-02-06
- Public Version Status
- Update
- Public Device Record Key
- cdd3a3ea-9f9a-4bf1-9ec4-dff270be2753
- Distribution End Date
- 2025-12-18
Device Description
MR Conditional Disposable EEG Cup Electrode System, 21 lead, black cup, CT compatible
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- MR Conditional
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| GXY | Electrode, Cutaneous | Neurology | 882.1320 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 11440 | Analytical scalp electrode, single-use | A noninvasive electrical conductor designed to be attached to the scalp surface of a patient to transmit changes in the electrical potential of various areas of the brain for recording/monitoring by a connected parent device [i.e., an electroencephalograph (EEG), sleep, or evoked potential recording device]. It typically consists of a small cup/disk with a conductive surface (e.g., tin, gold, conductive plastic) and a length of insulated connecting wire; it may be available as a set of multiple electrodes (e.g., EEG electrodes) however it is not a preconfigured EEG cap. This is a single-patient device that may be reapplied to the patient over a short term (single-use) before being discarded. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00850012681007 | GS1 | ||||
| Package | 00850012681120 | GS1 | Box | 10 | Not in Commercial Distribution | 2020-04-06 |
| Package | 10850012681004 | GS1 | Box | 10 | Not in Commercial Distribution | 2025-12-18 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K071118 | 000 |