FDA UDI In Commercial Distribution 🇺🇸 United States

Remote Monitoring

DI: 00887517213402 · Model: 8065010 · Nuvasive, Inc.
Product Codes
6
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Remote Monitoring
Primary DI
00887517213402
Version / Model
8065010
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-15
Public Version
3
Public Version Date
2025-06-11
Public Version Status
Update
Public Device Record Key
c982301d-7092-4308-b16e-666cf5243512

Device Description

Multimodality IOM Kit

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

GMDN Terms

Code Name
46566 Neurophysiologic monitoring system

Identifiers

Type ID
Primary 00887517213402

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K143641 000