FDA UDI In Commercial Distribution 🇺🇸 United States

OEC

DI: 00195278096944 · Model: 3D · OEC MEDICAL SYSTEMS, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OEC
Primary DI
00195278096944
Version / Model
3D
Catalog Number
00195278096944
Company Name
OEC MEDICAL SYSTEMS, INC.
Labeler DUNS
085305274
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-04-15
Public Version
2
Public Version Date
2022-07-22
Public Version Status
Update
Public Device Record Key
65c45b5b-1020-40cb-941c-7b2b2e33dcdd

Device Description

MEDICAL DEVICE, UDI LABEL PLACEMENT, OEC 3D

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
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
OXO Image-intensified fluoroscopic x-ray system, mobile

GMDN Terms

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

Identifiers

Type ID
Primary 00195278096944

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K203346 000