← Back to catalogue

ARIA Radiation Therapy Management

FDA UDI

Class II (US FDA UDI)

by Varian Medical Systems Imaging Laboratory GmbH

Identity

Trade Name
ARIA Radiation Therapy Management FDA UDI
Generic Name
Radiation therapy treatment record/verify system FDA UDI
Device Name
RTM FDA UDI
Model / Reference
15.0 FDA UDI
Description
RTM FDA UDI

Identifiers

Primary DI / UDI-DI
00856100006004 FDA UDI
510(k) Number
K133572 FDA UDI
FDA Product Code
IYE FDA UDI
GMDN Term
Radiation therapy treatment record/verify system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Category: Radiation therapy treatment record/verify system

ARIA Radiation Therapy Management by Varian Medical Systems Imaging Laboratory GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiation therapy treatment record/verify system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Varian Medical Systems Imaging Laboratory GmbH

Sources (1)

  • FDA UDI f046cdd2-5605-4d6e-8c3b-b19996136cbc 34 fields · synced Jun 8, 2026