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Varian Mobius Verification Phantom

FDA UDI

Class I (US FDA UDI)

by Varian Medical Systems, Inc

Identity

Trade Name
Varian Mobius Verification Phantom FDA UDI
Generic Name
Multi-modality therapeutic radiation phantom, anthropomorphic FDA UDI
Model / Reference
2.0 FDA UDI

Identifiers

Primary DI / UDI-DI
00899475002448 FDA UDI
FDA Product Code
IXG FDA UDI
GMDN Term
Multi-modality therapeutic radiation phantom, anthropomorphic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1950 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Multi-modality therapeutic radiation phantom, anthropomorphic

Varian Mobius Verification Phantom by Varian Medical Systems, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-modality therapeutic radiation phantom, anthropomorphic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Varian Medical Systems, Inc

Sources (1)

  • FDA UDI cfd29e71-db8e-4bc2-9491-8b0dcb964f3c 32 fields · synced May 30, 2026