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
GWF STIMULATOR, ELECTRICAL, EVOKED RESPONSE
OLO Orthopedic stereotaxic instrument
IKN Electromyograph, diagnostic
ETN STIMULATOR, NERVE
PDQ Neurosurgical nerve locator
HAW Neurological stereotaxic Instrument

GMDN Terms

Code Name
46566 Neurophysiologic monitoring system

Identifiers

Type ID
Primary 00887517824554

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K162313 000