Medium Torso Simulator

FDA UDI

Class II (US FDA UDI)

by Quality Electrodynamics Llc

Identity

Trade Name: MEDIUM TORSO SIMULATOR FDA UDI
Generic Name: Radiation therapy simulation system FDA UDI
Model / Reference: 2001001 FDA UDI

Identifiers

Catalog Number: MAC000112 FDA UDI
Primary DI / UDI-DI: 00814848020232 FDA UDI
FDA Product Code: IYE FDA UDI
GMDN Term: Radiation therapy simulation 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radiation therapy simulation system

Medium Torso Simulator by Quality Electrodynamics Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiation therapy simulation system.

Varian Acuity with Conebeam Computed Tomography — Varian Medical Systems, Inc · Class II
Acuity iX Radiation Therapy Simulation System — Varian Medical Systems, Inc · Class II
HEAD NECK SIMULATOR — QUALITY ELECTRODYNAMICS LLC · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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

Manufacturer

Manufacturer: Quality Electrodynamics Llc

Sources (1)

FDA UDI f7211c8a-2212-436c-a831-734b4a9a9229 33 fields · synced Jun 1, 2026