FDA UDI In Commercial Distribution 🇺🇸 United States

Nexxis

DI: 05415334002074 · Model: Nexxis OR · Barco NV
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Nexxis
Primary DI
05415334002074
Version / Model
Nexxis OR
Catalog Number
K9605012
Company Name
Barco NV
Labeler DUNS
371618773
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-24
Public Version
4
Public Version Date
2018-12-19
Public Version Status
Update
Public Device Record Key
7fa2ab8e-b52b-4506-9cc3-7fd6777e23fa

Device Description

4K ENC BUNDLE OL

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
Yes
PM Exempt
No
Has Serial Number
Yes
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
DXJ DISPLAY, CATHODE-RAY TUBE, MEDICAL

GMDN Terms

Code Name
58117 Operating room audiovisual data/device management system

Identifiers

Type ID
Primary 05415334002074

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K122167 000
K170537 000
K173381 000