DEPTHALON®
- Primary DI
- 00650551004455
- Brand
- DEPTHALON®
- Company
- PMT CORPORATION
- Model
- 2102-08-042
- Device description
- DEPTH ELECTRODE PLATINUM, 8 CONTACT, 5MM CONTACTS, MINI CONNECTOR
- Published
- 2025-03-15
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Related Records
Product Codes
| Code | Name |
|---|---|
| GZL | Electrode, Depth |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| GZL | Electrode, Depth | Neurology | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00650551004455 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00650551004455 | 00650551004455 | 650551004455 | 0650551004455 |
GMDN Terms
| Term | Definition |
|---|---|
| Depth electrode | An electrical conductor intended to be temporarily placed (< 30 days) beneath 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 fine, flexible plastic device attached to wires that carry currents from deep and superficial brain structures. The wires are connected to recording, monitoring, or stimulation/response devices [e.g., electroencephalograph (EEG), evoked-potential recorder, stimulator]. The implant is particularly helpful in determining site of origin in temporal and frontal lobe epilepsy. This is a single-use device. |
Sterilization Methods
| Method |
|---|
Regulatory Flags
- DUNS number
- 039576871
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- true
- Manufacturing date on label
- true
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- Sterilization required before use
- false
Other Devices From This Company
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00650551005445 | CORTAC® | 2110-06-005 | 2110-06-005 | 2025-04-25 |
| 00650551005452 | CORTAC® | 2110-08-006 | 2025-04-25 | |
| 00650551005469 | CORTAC® | 2110TX-16-008 | 2025-04-25 | |
| 00650551005476 | CORTAC® | 2110-32-005 | 2025-04-25 | |
| 00650551005391 | INTEGRA® | 3610ES-72-2I-ST | 2025-03-26 | |
| 00650551002086 | PMT® SUCTION INSTRUMENTS | 9001-06-225 | 2025-03-19 | |
| 00650551002093 | PMT® SUCTION INSTRUMENTS | 9002-08-225 | 2025-03-19 | |
| 00650551002154 | INTEGRA® | 3611-204-2I-ST | 2025-03-19 | |
| 00650551002161 | INTEGRA® | 3612-04-I-1T | 2025-03-19 | |
| 00650551002772 | INTEGRA® | 3610-76-2I-ST | 2025-03-19 | |
| 00650551002833 | INTEGRA® | 3612-06R-IR-ST | 2025-03-19 | |
| 00650551002932 | ALLURA® | 3321-214-T | 2025-03-19 | |
| 00650551002963 | INTEGRA® | 3612-61A-IR-ST7 | 2025-03-19 | |
| 00650551003083 | INTEGRA® | 3610-23-3 | 2025-03-19 | |
| 00650551003090 | INTEGRA® | 3611-674-3 | 2025-03-19 | |
| 00650551003168 | INTEGRA® | 3611ES-12-IR-ST | 2025-03-19 | |
| 00650551003175 | INTEGRA® | 3611ES-13-IR-ST | 2025-03-19 | |
| 00650551003182 | INTEGRA® | 3612ES-04R-IR-ST | 2025-03-19 | |
| 00650551003205 | INTEGRA® | 3610-579-2 | 2025-03-19 | |
| 00650551003212 | INTEGRA® | 3611-675-2 | 2025-03-19 |
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