← Back to catalogue

Blue Phantom²

FDA UDI

Class II (US FDA UDI)

by IBA Dosimetry GmbH

Identity

Trade Name
Blue Phantom² FDA UDI
Generic Name
Accelerator system quality assurance device FDA UDI
Device Name
Blue Phantom² thin window, leveling FDA UDI
Model / Reference
M1013681 FDA UDI
Description
Blue Phantom² thin window, leveling FDA UDI

Identifiers

Primary DI / UDI-DI
EIBAM10136810 FDA UDI
FDA Product Code
IYE FDA UDI
GMDN Term
Accelerator system quality assurance device 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Accelerator system quality assurance device

Blue Phantom² by IBA Dosimetry GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Accelerator system quality assurance device.

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
IBA Dosimetry GmbH

Sources (1)

  • FDA UDI b5d09461-6449-40bc-a86e-936d393f4b80 34 fields · synced May 30, 2026