FDA UDI In Commercial Distribution 🇺🇸 United States

PULSE

DI: 00887517990761 · Model: BETPULSECAMERACART · Nuvasive, Inc.
Product Codes
9
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PULSE
Primary DI
00887517990761
Version / Model
BETPULSECAMERACART
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-18
Public Version
1
Public Version Date
2019-11-26
Public Version Status
New
Public Device Record Key
f9cb25d3-2f80-4d57-9aca-4b81f7c45c1c

Device Description

PULSE Camera Cart, BETA

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
No

Product Codes

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

GMDN Terms

Code Name
45200 Orthopaedic stereotactic surgery system

Identifiers

Type ID
Primary 00887517990761

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K180038 000