FDA UDI In Commercial Distribution 🇺🇸 United States

AMX

DI: 00195278798374 · Model: NAVIGATE UPGRADE · GE MEDICAL SYSTEMS, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AMX
Primary DI
00195278798374
Version / Model
NAVIGATE UPGRADE
Company Name
GE MEDICAL SYSTEMS, INC.
Labeler DUNS
809785715
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-24
Public Version
1
Public Version Date
2024-02-01
Public Version Status
New
Public Device Record Key
afb25c68-a4ae-4107-b56d-60f4fda85f23

Device Description

AMX Navigate Upgrade Designated Medical Device Assembly

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
IZL System, x-ray, mobile
MQB Solid state x-ray imager (flat panel/digital imager)

GMDN Terms

Code Name
37647 Mobile basic diagnostic x-ray system, digital

Identifiers

Type ID
Primary 00195278798374

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K210982 000