FDA UDI In Commercial Distribution 🇺🇸 United States

OneRF Ablation System

DI: 00856895008511 · Model: NRFBK0001 · NEUROONE MEDICAL TECHNOLOGIES CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
OneRF Ablation System
Primary DI
00856895008511
Version / Model
NRFBK0001
Company Name
NEUROONE MEDICAL TECHNOLOGIES CORPORATION
Labeler DUNS
105937669
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-15
Public Version
1
Public Version Date
2024-03-25
Public Version Status
New
Public Device Record Key
8e6cc849-f00f-47b0-9034-f210ad97600f

Device Description

Generator Accessory - Bin

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GXD Generator, Lesion, Radiofrequency

GMDN Terms

Code Name
35156 Percutaneous radio-frequency ablation system generator

Identifiers

Type ID
Primary 00856895008511