SafeOp 3
- Primary DI
- 00190376537115
- Brand
- SafeOp 3
- Company
- ALPHATEC SPINE, INC.
- Model
- AIX12105
- Device description
- SafeOp 3 Electrode Kit – EMG Only - Surface
- Published
- 2024-11-12
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| GXY | Electrode, cutaneous |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| GXY | Electrode, Cutaneous | Neurology | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K234092 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00190376537115 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00190376537115 | 00190376537115 | 190376537115 | 0190376537115 |
GMDN Terms#
| Term | Definition |
|---|---|
| Analytical non-scalp cutaneous electrode | An electrical conductor designed to be attached to the skin surface of a patient outside of the hair line (i.e., non-scalp) to conduct electrical signals to/from a parent device for electrophysiological recording/monitoring [e.g., electromyography (EMG), evoked potentials (EP), nerve conduction study (NCS), bioelectrical impedance]; it is not primarily intended for diagnostic electrocardiography (ECG) or electroencephalography (EEG). It typically consists of a small rectangular tab or cup/disk with a conductive surface, which may include a lead wire. This is a single-patient device that may be reapplied to the patient over a short term (single-use) before being discarded. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(760)431-9286 | Regulatory@alphatecspine.com |
Regulatory Flags#
- DUNS number
- 602465783
- Device count
- 1
- DM exempt
- true
- Kit
- true
- Lot or batch
- true
- Manufacturing date on label
- true
- No natural rubber latex
- true
Other Devices From This Company#
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|---|---|---|---|---|
| 00190376541471 | ATEC Lateral Navigation Disc Prep Instruments | 267-01-000-10-N | 2024-12-18 | |
| 00190376529158 | ATEC Posterior Navigation Disc Prep Instruments | 244-01-000-06-N | 2024-04-20 | |
| 00190376529189 | ATEC Posterior Navigation Disc Prep Instruments | 244-01-000-12-N | 2024-04-20 | |
| 00190376476162 | ATEC Lateral Navigation Disc Prep Instruments | 266-01-000-08-N | 2023-08-26 | |
| 00190376476179 | ATEC Lateral Navigation Disc Prep Instruments | 266-01-000-10-N | 2023-08-26 | |
| 00190376476186 | ATEC Lateral Navigation Disc Prep Instruments | 266-01-000-12-N | 2023-08-26 | |
| 00190376522906 | ATEC Lateral Navigation Disc Prep Instruments | 266-01-000-14-N | 2023-08-26 | |
| 00840180512395 | General Instruments | CI-11129-3424 | 2026-05-15 | |
| 00840180543214 | General Instruments | CI-11899 | 2026-05-15 | |
| 00840180543542 | General Instruments | CI-11915-30 | 2026-05-15 | |
| 00840180544785 | General Instruments | CI-11939-080-R | 2026-05-15 | |
| 00840180544914 | General Instruments | CI-11939-080-L | 2026-05-15 | |
| 00840180545324 | General Instruments | CI-11968-06-S | 2026-05-15 | |
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