FDA UDI In Commercial Distribution 🇺🇸 United States

NVJJB

DI: 00887517206152 · Model: 8010070 · Nuvasive, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NVJJB
Primary DI
00887517206152
Version / Model
8010070
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-26
Public Version
4
Public Version Date
2023-12-18
Public Version Status
Update
Public Device Record Key
e2a909fc-d118-4d41-ab3e-213b5aa730ca

Device Description

NVJJB Module II Electrodes, Wet Gel

Device Characteristics

Single Use
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
ETN STIMULATOR, NERVE
GWF STIMULATOR, ELECTRICAL, EVOKED RESPONSE
IKN Electromyograph, diagnostic

GMDN Terms

Code Name
61020 Analytical non-scalp cutaneous electrode

Identifiers

Type ID
Primary 00887517206152

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K112717 000