FDA UDI In Commercial Distribution 🇺🇸 United States

OEC

DI: 00840682114301 · Model: 9900 ELITE · OEC MEDICAL SYSTEMS, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OEC
Primary DI
00840682114301
Version / Model
9900 ELITE
Company Name
OEC MEDICAL SYSTEMS, INC.
Labeler DUNS
085305274
Distribution Status
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
da896934-c723-44b5-b97e-e9a78961438f

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
OWB Interventional fluoroscopic x-ray system
OXO Image-intensified fluoroscopic x-ray system, mobile
JAA System, x-ray, fluoroscopic, image-intensified

GMDN Terms

Code Name
37646 Mobile general-purpose fluoroscopic x-ray system, digital

Identifiers

Type ID
Primary 00840682114301

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K082781 000
K120613 000
K122234 000