FDA UDI Not in Commercial Distribution 🇺🇸 United States

RemotEye Viewer

DI: B383REV090202000 · Model: 9.2.2 · NEOLOGICA SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RemotEye Viewer
Primary DI
B383REV090202000
Version / Model
9.2.2
Company Name
NEOLOGICA SRL
Labeler DUNS
517480120
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-07
Public Version
6
Public Version Date
2024-01-19
Public Version Status
Update
Public Device Record Key
4c8f2a68-72c1-46f4-8e9a-f8e31dccd053
Distribution End Date
2018-10-31

Device Description

Diagnostic web DICOM viewer

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
Yes
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
41670 Radiological PACS software

Identifiers

Type ID
Primary B383REV090202000

Customer Contacts

Phone
+39019505314

Premarket Submissions

Submission Number Supplement Number
K141061 000