FDA UDI Not in Commercial Distribution 🇺🇸 United States

DISCOVERY

DI: 00840682104739 · Model: IGS 730 001 · GE MEDICAL SYSTEMS
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DISCOVERY
Primary DI
00840682104739
Version / Model
IGS 730 001
Company Name
GE MEDICAL SYSTEMS
Labeler DUNS
266062561
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-01
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
36de6348-423c-43bf-a48d-6ef120450394
Distribution End Date
2016-08-02

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
No
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
JAA System, x-ray, fluoroscopic, image-intensified
IZI System, x-ray, angiographic

GMDN Terms

Code Name
37623 Stationary angiographic x-ray system, digital

Identifiers

Type ID
Primary 00840682104739

Premarket Submissions

Submission Number Supplement Number
K122457 000