FDA UDI In Commercial Distribution 🇺🇸 United States

Automatic Registration

DI: 04056481145101 · Model: 2.6 · Brainlab AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Automatic Registration
Primary DI
04056481145101
Version / Model
2.6
Company Name
Brainlab AG
Labeler DUNS
314482980
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-22
Public Version
1
Public Version Date
2023-10-02
Public Version Status
New
Public Device Record Key
33d50b19-2b8e-4222-8b98-8e75ff2e8d85

Device Description

Trade names: AUTO-REGISTRATION SOFTWARE AIRO CRANIAL, AUTO-REGISTRATION SOFTWARE AIRO CMF, AUTO-REGISTRATION SOFTWARE LOOP-X CRANIAL, AUTO-REGISTRATION SOFTWARE LOOP-X CMF, AUTO-REGISTRATION SOFTWARE UNIVERSAL AIR CRANIAL, AUTO-REGISTRATION SOFTWARE UNIVERSAL AIR CMF,

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
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
HAW Neurological Stereotaxic Instrument

GMDN Terms

Code Name
62783 Electromagnetic/optical surgical navigation device tracking system

Identifiers

Type ID
Primary 04056481145101

Premarket Submissions

Submission Number Supplement Number
K223288 000
K223864 000