← Back to catalogue

End-To-End SRS Head Phantom

FDA UDI

Class I (US FDA UDI)

by Varian Medical Systems, Inc

Identity

Trade Name
End-To-End SRS Head Phantom FDA UDI
Generic Name
Multi-modality therapeutic radiation phantom, anthropomorphic FDA UDI
Model / Reference
1.0 FDA UDI

Identifiers

Primary DI / UDI-DI
00899475002455 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Multi-modality therapeutic radiation phantom, anthropomorphic

End-To-End SRS Head 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

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

Manufacturer

Manufacturer
Varian Medical Systems, Inc

Sources (1)

  • FDA UDI 13e27a52-d331-4132-a72f-f551ecd77d4f 32 fields · synced May 30, 2026