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Standard Imaging IMRT Dose Verification Phantom

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 91230

by Standard Imaging, Inc.

Identity

Trade Name
IMRT Phantom EUDAMED
Standard Imaging IMRT Dose Verification Phantom FDA UDI
Generic Name
Multi-modality therapeutic radiation phantom, test object FDA UDI
Device Name
IMRT Phantom EUDAMED
Standard Imaging IMRT Phantoms are designed to provide feedback on complex treatment plans generated using 3D. The phantoms are designed to mimic a human torso. Both film and ion chambers can be simultaneously irradiated for comparisons with the treatment planning system. FDA UDI
Model / Reference
91230 EUDAMEDFDA UDI
Description
Standard Imaging IMRT Phantoms are designed to provide feedback on complex treatment plans generated using 3D. The phantoms are designed to mimic a human torso. Both film and ion chambers can be simultaneously irradiated for comparisons with the treatment planning system. FDA UDI

Identifiers

Catalog Number
91230 FDA UDI
Primary DI / UDI-DI
00850019946550 EUDAMEDFDA UDI
Basic UDI-DI
0850019946IMRTPHANTOMLR EUDAMED
FDA Product Code
IXG FDA UDI
EMDN Code
Z11019080 VARIOUS RADIOTHERAPY AND RADIOSURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Multi-modality therapeutic radiation phantom, test object FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
892.1950 FDA UDI
Market of Registration
France EUDAMED
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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Multi-modality therapeutic radiation phantom, test object

Standard Imaging IMRT Dose Verification Phantom by Standard Imaging, Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Multi-modality therapeutic radiation phantom, test object.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI cf3d9a03-250d-4c22-a29d-b0e6cbc16ec6 34 fields · synced Jul 15, 2026
  • EUDAMED 2dfbd836-d8ef-4fe8-b933-a4d2806adec5 61 fields · synced Jul 15, 2026