Elekta Medical Linear Accelerator

FDA UDI

Class II (US FDA UDI)

by Elekta Solutions AB

Identity

Trade Name: Elekta Medical Linear Accelerator FDA UDI
Generic Name: Linear accelerator system FDA UDI
Device Name: Versa HD™ FDA UDI
Model / Reference: 1552093 FDA UDI
Description: Versa HD™ FDA UDI

Identifiers

Primary DI / UDI-DI: 05060191071574 FDA UDI
FDA Product Code: IYE FDA UDI
GMDN Term: Linear accelerator 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: Linear accelerator system

Elekta Medical Linear Accelerator by Elekta Solutions AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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

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Manufacturer

Manufacturer: Elekta Solutions AB

Sources (1)

FDA UDI 07927283-27b1-49f4-8187-f5419673eaf2 34 fields · synced May 30, 2026