FDA UDI In Commercial Distribution 🇺🇸 United States

PULSE

DI: 00195377060686 · Model: PULSEDRILLGUIDE · Nuvasive, Inc.
Product Codes
9
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PULSE
Primary DI
00195377060686
Version / Model
PULSEDRILLGUIDE
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-05-06
Public Version
1
Public Version Date
2022-05-16
Public Version Status
New
Public Device Record Key
732eb947-346b-4e21-8850-4abb98cb5aea

Device Description

Pulse Drill Guide

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GWF STIMULATOR, ELECTRICAL, EVOKED RESPONSE
IKN Electromyograph, diagnostic
OLO Orthopedic stereotaxic instrument
JAA System, x-ray, fluoroscopic, image-intensified
PDQ Neurosurgical nerve locator
OWB Interventional fluoroscopic x-ray system
LLZ System, image processing, radiological
HAW Neurological stereotaxic Instrument
ETN STIMULATOR, NERVE

GMDN Terms

Code Name
45200 Orthopaedic stereotactic surgery system

Identifiers

Type ID
Primary 00195377060686

Customer Contacts