FDA UDI In Commercial Distribution 🇺🇸 United States

Prelude

DI: 04260308110078 · Model: V1. · MedCom Gesellschaft für medizinische Bildverarbeitung mbH
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Prelude
Primary DI
04260308110078
Version / Model
V1.
Company Name
MedCom Gesellschaft für medizinische Bildverarbeitung mbH
Labeler DUNS
537689275
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-02
Public Version
1
Public Version Date
2020-06-10
Public Version Status
New
Public Device Record Key
c454c0c6-b6e6-4956-bcdc-9016bf97c3f5

Device Description

The Prelude software supports intra-operative radiation therapy workflows with intra-operative radiation devices like IntraOp Mobetron. It assists to find product specific machine parameters for treatment and can send those proposals to the intra-operative radiation device. The machine parameters are not intended to be used for direct control for the radiation device. Machine Output Quality can be visualized and recorded over time for quality assurance.

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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LHO Instrument, Quality-Assurance, Radiologic
MUJ System, Planning, Radiation Therapy Treatment

GMDN Terms

Code Name
40887 Radiation therapy software

Identifiers

Type ID
Primary 04260308110078

Premarket Submissions

Submission Number Supplement Number
K180308 000