FDA UDI In Commercial Distribution 🇺🇸 United States

INNOVA

DI: 00840682110129 · Model: IGS 520 002 · GE MEDICAL SYSTEMS
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
INNOVA
Primary DI
00840682110129
Version / Model
IGS 520 002
Company Name
GE MEDICAL SYSTEMS
Labeler DUNS
266062561
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-01
Public Version
4
Public Version Date
2021-11-30
Public Version Status
Update
Public Device Record Key
cd85c775-461a-4a7b-9bbb-4fc426211695

Device Description

INNOVA IGS 520 002

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
No
Has Serial Number
Yes
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
OWB Interventional fluoroscopic x-ray system
IZI System, x-ray, angiographic
JAA System, x-ray, fluoroscopic, image-intensified

GMDN Terms

Code Name
37623 Stationary angiographic x-ray system, digital

Identifiers

Type ID
Primary 00840682110129

Premarket Submissions

Submission Number Supplement Number
K122457 000