FDA UDI
In Commercial Distribution
🇺🇸 United States
PULSE
DI: 00887517824554
·
Model: 50120201
·
Nuvasive, Inc.
Product Codes
6
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- PULSE
- Primary DI
- 00887517824554
- Version / Model
- 50120201
- Company Name
- Nuvasive, Inc.
- Labeler DUNS
- 053950783
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2018-06-26
- Public Version
- 1
- Public Version Date
- 2018-07-27
- Public Version Status
- New
- Public Device Record Key
- 97858bc7-a46c-4696-bdaa-9f030a46923e
Device Description
EMG Electrode Kit, Surface
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- Yes
- 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
- Yes
- 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 |
|---|---|---|---|---|
| GWF | STIMULATOR, ELECTRICAL, EVOKED RESPONSE | Neurology | 882.1870 | 2 |
| OLO | Orthopedic stereotaxic instrument | Neurology | 882.4560 | 2 |
| IKN | Electromyograph, diagnostic | Physical Medicine | 890.1375 | 2 |
| ETN | STIMULATOR, NERVE | Ear, Nose, Throat | 874.1820 | 2 |
| PDQ | Neurosurgical nerve locator | Ear, Nose, Throat | 874.1820 | 2 |
| HAW | Neurological stereotaxic Instrument | Neurology | 882.4560 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 46566 | Neurophysiologic monitoring system | An assembly of mains electricity (AC-powered) devices designed to monitor and provide electrical stimuli to spinal nerves or other neural pathways (may include the brain) during intraoperative surgery or intensive care, typically to reduce the incidence of accidental injury during instrumented spine surgery, or to diagnose acute dysfunction in corticospinal conduction (e.g., due to traction, shearing, laceration, compression, or vascular insufficiency). It typically displays electroencephalogram (EEG), electromyogram (EMG), and/or evoked responses. It typically includes an electric current pulse generator, electrodes and/or probes, and audible and/or visual indicators. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00887517824554 | GS1 |
Customer Contacts
- Phone
- +1(858)909-1800
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K162313 | 000 |