FDA UDI
In Commercial Distribution
🇺🇸 United States
FREMAP Electrode
DI: 00841823108487
·
Model: DCNE-01-05X
·
Ad-Tech Medical Instrument Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1
Basic Information
- Brand Name
- FREMAP Electrode
- Primary DI
- 00841823108487
- Version / Model
- DCNE-01-05X
- Catalog Number
- DCNE-01-05X
- Company Name
- Ad-Tech Medical Instrument Corporation
- Labeler DUNS
- 174813410
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2016-10-03
- Public Version
- 4
- Public Version Date
- 2023-08-23
- Public Version Status
- Update
- Public Device Record Key
- 6632dbc8-839a-49e7-9404-a8f210998ccb
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
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| ETN | STIMULATOR, NERVE | Ear, Nose, Throat | 874.1820 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 32545 | Cortical electrode | A sterile, invasive, electrical conductor that is temporarily placed (< 30 days) on the surface of the brain to stimulate the brain or to record the brain's electrical activity (with more precise localization than a scalp electrode). It is typically a series of discs mounted in thin plastic strips, or in a square/rectangular grid to cover larger surface areas. The implanted device, also known as a subdural electrode, is connected to recording, monitoring, or stimulation/response devices [e.g., electroencephalograph (EEG), evoked-potential recorder, stimulator]. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 90841823108480 | GS1 | 5 | In Commercial Distribution | ||
| Primary | 00841823108487 | GS1 |
Customer Contacts
- Phone
- +1(800)776-1555
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K152769 | 000 |
Storage Conditions
- Type
- Special Storage Condition, Specify
- Special Conditions
- To be stored and used within typical hospital/office room ambient temperature and humidity conditions