FDA UDI In Commercial Distribution 🇺🇸 United States

Nexstim NBT system

DI: 06430063200149 · Model: 2 · NEXSTIM, INC.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Nexstim NBT system
Primary DI
06430063200149
Version / Model
2
Company Name
NEXSTIM, INC.
Labeler DUNS
010845069
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-28
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
b62ca342-fcdf-4c2b-b79d-12bb1995f8b1

Device Description

Nexstim NBT system

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GWF Stimulator, Electrical, Evoked Response
IKN Electromyograph, Diagnostic
HAW Neurological Stereotaxic Instrument
OBP Transcranial Magnetic Stimulator

GMDN Terms

Code Name
56641 Stereotactic neuronavigation/planning system

Identifiers

Type ID
Primary 06430063200149

Customer Contacts

Phone
+35892727170