FDA UDI In Commercial Distribution 🇺🇸 United States

Scorpion

DI: B006IDKMF512B52 · Model: N/A · NEUROVISION MEDICAL PRODUCTS, INC.
Product Codes
2
GMDN Terms
2
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
Scorpion
Primary DI
B006IDKMF512B52
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
2021-11-17
Public Version
2
Public Version Date
2023-12-25
Public Version Status
Update
Public Device Record Key
9093c963-d9c9-42c5-aa83-e2d114eb4750

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
Yes
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
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
ETN Stimulator, Nerve
IKT Electrode, Needle, Diagnostic Electromyograph

GMDN Terms

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

Identifiers

Type ID
Package IDKMF512B5
Primary B006IDKMF512B52
Unit of Use B006IDKMF512B5