FDA UDI In Commercial Distribution 🇺🇸 United States

UltraPREFETCH

DI: 00860001148558 · Model: 3.0.3.2 · ULTRARAD CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
UltraPREFETCH
Primary DI
00860001148558
Version / Model
3.0.3.2
Company Name
ULTRARAD CORPORATION
Labeler DUNS
139399021
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-02-13
Public Version
3
Public Version Date
2023-10-18
Public Version Status
Update
Public Device Record Key
cfec958d-ae8d-46ce-8bc1-158d54881fe2

Device Description

UltraPREFETCH automatically retrieves studies and sends to any DICOM client, on a rule based criteria.

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
LLZ System, Image Processing, Radiological

GMDN Terms

Code Name
41670 Radiological PACS software

Identifiers

Type ID
Primary 00860001148558

Customer Contacts

Phone
800-527-3779

Premarket Submissions

Submission Number Supplement Number
K051813 000