FDA UDI In Commercial Distribution 🇺🇸 United States

PREIRUS

DI: 04961333243105 · Model: HITACHI5.1UPGRD · PENTAX OF AMERICA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PREIRUS
Primary DI
04961333243105
Version / Model
HITACHI5.1UPGRD
Company Name
PENTAX OF AMERICA, INC.
Labeler DUNS
083211284
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-12
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
e9d6a430-b7d0-4206-96e1-a115e0ab9bd1

Device Description

HITACHI 5.1 SOFTWARE UPGRADE PREIRUS

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IYO System, Imaging, Pulsed Echo, Ultrasonic

GMDN Terms

Code Name
40761 General-purpose ultrasound imaging system

Identifiers

Type ID
Primary 04961333243105

Premarket Submissions

Submission Number Supplement Number
K093466 000