FDA UDI In Commercial Distribution 🇺🇸 United States

Digital Capture v3.7.0

DI: 04961333255696 · Model: 9380 · PENTAX OF AMERICA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Digital Capture v3.7.0
Primary DI
04961333255696
Version / Model
9380
Company Name
PENTAX OF AMERICA, INC.
Labeler DUNS
083211284
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-12
Public Version
1
Public Version Date
2025-09-22
Public Version Status
New
Public Device Record Key
349472c5-9582-40d4-8451-18c5874b7e00

Device Description

9380 Digital Capture Software

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OUG Medical Device Data System

GMDN Terms

Code Name
60723 Medical image management system

Identifiers

Type ID
Primary 04961333255696