FDA UDI In Commercial Distribution 🇺🇸 United States

ATLAS COMBO BOARD

DI: 00850011306147 · Model: ATLAS COMBO BOARD · NEURALYNX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ATLAS COMBO BOARD
Primary DI
00850011306147
Version / Model
ATLAS COMBO BOARD
Catalog Number
31-0605-0117
Company Name
NEURALYNX, INC.
Labeler DUNS
933200842
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-02-27
Public Version
2
Public Version Date
2023-07-12
Public Version Status
Update
Public Device Record Key
f18a0497-1704-40ce-9ad6-08c17c62d113

Device Description

The ATLAS Combo Board combines the functionality of the ATLAS Hybrid Input Board and ATLAS DRS-36 Board onto a single board, meaning the Digital Reference Selection and Analog to Digital Conversion for 32 electrodes is combined into a single slot.

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
OMC Reduced- Montage Standard Electroencephalograph

GMDN Terms

Code Name
38736 Electroencephalographic monitoring system

Identifiers

Type ID
Primary 00850011306147

Customer Contacts

Phone
4065854542

Premarket Submissions

Submission Number Supplement Number
K110967 000