FDA UDI In Commercial Distribution 🇺🇸 United States

DCX

DI: 00869126000468 · Model: DCX · OSKO, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DCX
Primary DI
00869126000468
Version / Model
DCX
Company Name
OSKO, INC.
Labeler DUNS
017527767
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-06-10
Public Version
1
Public Version Date
2019-06-18
Public Version Status
New
Public Device Record Key
bcc7713b-6697-4b33-80b8-0b4fcd95022b

Device Description

Stationary X-Ray System

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KPR System, X-Ray, Stationary

GMDN Terms

Code Name
37644 Stationary basic diagnostic x-ray system, analogue

Identifiers

Type ID
Primary 00869126000468

Customer Contacts

Phone
+13055997161

Premarket Submissions

Submission Number Supplement Number
K150663 000