FDA UDI In Commercial Distribution 🇺🇸 United States

Cobra®

DI: B006LTE7003PMD52 · Model: N/A · NEUROVISION MEDICAL PRODUCTS, INC.
Product Codes
5
GMDN Terms
3
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
Cobra®
Primary DI
B006LTE7003PMD52
Version / Model
N/A
Company Name
NEUROVISION MEDICAL PRODUCTS, INC.
Labeler DUNS
182057401
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2023-04-06
Public Version
1
Public Version Date
2023-04-14
Public Version Status
New
Public Device Record Key
c196d9ea-6c7a-44d1-b673-fa09db784e2d

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
ETN Stimulator, Nerve
BTR Tube, Tracheal (W/Wo Connector)
GWF Stimulator, Electrical, Evoked Response
GXZ Electrode, Needle
IKT Electrode, Needle, Diagnostic Electromyograph

GMDN Terms

Code Name
61070 Electromyographic endotracheal tube
61089 Nerve-locating system probe, single-use
11441 Electromyographic needle electrode, single-use

Identifiers

Type ID
Unit of Use B006LTE7003PMD1
Primary B006LTE7003PMD52
Package LTE7003PMD5