FDA UDI In Commercial Distribution 🇺🇸 United States

Hermia

DI: 00859873006189 · Model: 00859873006189 · Hermes Medical Solutions AB
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Hermia
Primary DI
00859873006189
Version / Model
00859873006189
Company Name
Hermes Medical Solutions AB
Labeler DUNS
354140220
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-10
Public Version
2
Public Version Date
2026-03-11
Public Version Status
Update
Public Device Record Key
2aafdb7f-972f-41c5-9112-25f6684991bb

Device Description

Hybrid Viewer is a software application for nuclear medicine and radiology. Based on user input, Hybrid Viewer processes, displays and analyzes nuclear medicine and radiology imaging data and presents the results to the user. The results can be stored for future analysis. Hybrid Viewer is equipped with dedicated workflows which have predefined settings and layouts optimized for specific nuclear medicine investigations. The software application can be configured based on user needs. The investigation of physiological or pathological states using measurement and analysis functionality provided by Hybrid Viewer is not intended to replace visual assessment. The information obtained from viewing and/or performing quantitative analysis on the images is used, in conjunction with other patient related data, to inform clinical management.

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
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
KPS System, Tomography, Computed, Emission

GMDN Terms

Code Name
40937 Nuclear medicine system workstation

Identifiers

Type ID
Primary 00859873006189

Premarket Submissions

Submission Number Supplement Number
K241364 000