FDA UDI In Commercial Distribution 🇺🇸 United States

Konica Minolta SW (PACS) Exa

DI: 00817100020193 · Model: EXA 01-04-000 · KONICA MINOLTA MEDICAL IMAGING U.S.A., INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Konica Minolta SW (PACS) Exa
Primary DI
00817100020193
Version / Model
EXA 01-04-000
Company Name
KONICA MINOLTA MEDICAL IMAGING U.S.A., INC.
Labeler DUNS
080269345
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2019-02-21
Public Version Status
Update
Public Device Record Key
befc67c1-dfee-4b4c-b48a-9c2b7cb98516

Device Description

EXA is a software device that receives digital images and data from various sources (i.e. CT scanners, MR scanners, ultrasound systems, R/F Units, computed & direct radiographic devices, secondary capture devices, scanners, imaging gateways or other imaging sources). Images and data can be stored, communicated, processed and displayed within the system and or across computer networks at distributed locations. Lossy compressed mammographic images are not intended for diagnostic review.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
LLZ System, Image Processing, Radiological

GMDN Terms

Code Name
40935 Diagnostic x-ray digital imaging system workstation

Identifiers

Type ID
Primary 00817100020193

Customer Contacts