FDA UDI In Commercial Distribution 🇺🇸 United States

Cobra

DI: B006LTE7003PL52 · Model: N/A · NEUROVISION MEDICAL PRODUCTS, INC.
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
Cobra
Primary DI
B006LTE7003PL52
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
2020-08-12
Public Version
1
Public Version Date
2020-08-20
Public Version Status
New
Public Device Record Key
041635ab-c3d8-4a42-b11e-335e14f1a785

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
Yes
MRI Safety
MR Unsafe
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
No
Sterilization Prior Use
No

Product Codes

Code Name
GWF Stimulator, Electrical, Evoked Response
ETN Stimulator, Nerve
BTR Tube, Tracheal (W/Wo Connector)

GMDN Terms

Code Name
61070 Electromyographic endotracheal tube

Identifiers

Type ID
Unit of Use B006LTE7003PL1
Primary B006LTE7003PL52

Premarket Submissions

Submission Number Supplement Number
K110989 000