FDA UDI In Commercial Distribution 🇺🇸 United States

Atlantis

DI: 00852391007027 · Model: Atlantis 4x4 · BRAINMASTER TECHNOLOGIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Atlantis
Primary DI
00852391007027
Version / Model
Atlantis 4x4
Catalog Number
390-030
Company Name
BRAINMASTER TECHNOLOGIES, INC.
Labeler DUNS
008607256
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-15
Public Version
1
Public Version Date
2023-08-23
Public Version Status
New
Public Device Record Key
4d5ca841-2f8d-4df4-8754-8e9534ce783b

Device Description

EEG Amplifier

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HCC Device, Biofeedback

GMDN Terms

Code Name
11467 Electroencephalograph

Identifiers

Type ID
Primary 00852391007027

Customer Contacts

Phone
440 232-6000