← Back to catalogue

RT Elements - (Elements) Multiple Brain Mets SRS

FDA 510(k)FDA UDIEUDAMED

Class II (US FDA 510(k))

510(k) K250440Ref 04056481146030

by Brainlab AG

Identity

Trade Name
RT Elements, 4.5 EUDAMED
RT Elements FDA UDI
Generic Name
Radiation therapy software FDA UDI
Device Name
RT Elements EUDAMED
Model / Reference
04056481146030 EUDAMED
4.5 FDA UDI

Identifiers

Primary DI / UDI-DI
04056481146030 EUDAMEDFDA UDI
Basic UDI-DI
4056481RTElementsW8 EUDAMED
Direct Marketing DI
04056481146030 EUDAMED
510(k) Number
K250440 FDA 510(k)FDA UDI
FDA Product Code
MUJ FDA 510(k)FDA UDI
QIH FDA UDI
EMDN Code
Z11010492 RADIOTHERAPY TREATMENT PLANNING INSTRUMENTS - MEDICAL DEVICE SOFTWARE EUDAMED
GMDN Term
Radiation therapy software FDA UDI
Models / Variants
RT Elements (4.5) FDA 510(k)FDA UDIEUDAMED
(Elements) Multiple Brain Mets SRS FDA 510(k)FDA UDIEUDAMED
(Elements) Cranial SRS FDA 510(k)FDA UDIEUDAMED
(Elements) Spine SRS FDA 510(k)FDA UDIEUDAMED
(Elements) Cranial SRS w/ Cones FDA 510(k)FDA UDIEUDAMED
(Elements) RT Planning Platform FDA 510(k)FDA UDIEUDAMED
(Elements) Dose Review FDA 510(k)FDA UDIEUDAMED
(Elements) Retreatment Review FDA 510(k)FDA UDIEUDAMED
Elements AI Tumor Segmentation RT FDA 510(k)FDA UDIEUDAMED
Elements SmartBrush [Angio, Spine] RT FDA 510(k)FDA UDIEUDAMED
Elements Object Management RT FDA 510(k)FDA UDIEUDAMED

Classification

Device Class
Class IIb EUDAMED
Class II FDA 510(k)FDA UDI
Legislation / Framework
21 CFR Part 892.5050 FDA 510(k)
Regulation Number
892.5050 FDA 510(k)FDA UDI
892.2050 FDA UDI
Special Device Type
Software EUDAMED
Market of Registration
Germany EUDAMED
Advisory Committee
Radiology FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

RT Elements is a software suite for radiation therapy (RT) treatment planning, designed under the OpenFDA classification as a System, Planning, Radiation Therapy Treatment device. It integrates multiple specialized modules—including stereotactic radiosurgery (SRS) tools for brain metastases, cranial and spine applications, and advanced segmentation and dose review functionalities—to support precise target delineation, adaptive planning, and treatment optimization across various anatomical regions.

The system is supplied as a digital software platform, intended for use in radiology departments and radiation oncology clinics. It operates as a reusable, non-sterile solution with no MRI safety considerations specified. Modules cover indications such as cranial, basal ganglia, head & neck, pelvic, and extracranial regions, with AI-assisted tumor segmentation and smart brush tools for enhanced workflow efficiency. Authorized under FDA 510(k) and MDR compliance, it adheres to regulatory standards for radiation therapy planning systems.

This description and any FAQs above were generated automatically from registry data and have not been verified by the manufacturer or by deviCERTS. Always check the official registry entry and the manufacturer's instructions for use before relying on them. Sources consulted: RT Elements (4.5); (Elements) Multiple Brain Mets SRS; (Elements ..., Elements: Radiotherapy & Radiosurgery Treatment Planning | Brainlab, RT Elements (4.5); (Elements) Multiple Brain Mets SRS; (Elements ...

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

MDR

United States Active

FDA_510K

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Brainlab AG

Sources (3)

  • FDA 510(k) K250440 24 fields · synced Sep 18, 2026
  • FDA UDI e6c53577-e093-4cdf-bb59-9bde37dfdcd9 33 fields · synced May 30, 2026
  • EUDAMED dc38133b-496a-4cd4-b693-aee6e3ee50e0 61 fields · synced Jul 9, 2026