Leksell GammaPlan

GUDID 07340201503898

Leksell GammaPlan 11.5

Elekta Solutions AB

Stereotactic system application software
Primary Device ID07340201503898
NIH Device Record Key7578432a-d5f8-4aa5-8ee7-3093bb942df8
Commercial Distribution StatusIn Commercial Distribution
Brand NameLeksell GammaPlan
Version Model Number1577756
Company DUNS353272181
Company NameElekta Solutions AB
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone8556935358
Emailinfo.america@elekta.com
Phone8556935358
Emailinfo.america@elekta.com
Phone8556935358
Emailinfo.america@elekta.com
Phone8556935358
Emailinfo.america@elekta.com
Phone8556935358
Emailinfo.america@elekta.com
Phone8556935358
Emailinfo.america@elekta.com
Phone8556935358
Emailinfo.america@elekta.com
Phone8556935358
Emailinfo.america@elekta.com
Phone8556935358
Emailinfo.america@elekta.com
Phone8556935358
Emailinfo.america@elekta.com
Phone8556935358
Emailinfo.america@elekta.com
Phone8556935358
Emailinfo.america@elekta.com

Device Identifiers

Device Issuing AgencyDevice ID
GS107340201503898 [Primary]

FDA Product Code

IWBSystem, Radiation Therapy, Radionuclide

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-02-12
Device Publish Date2026-02-04

On-Brand Devices [Leksell GammaPlan]

07340201502136Leksell GammaPlan
07340201503898Leksell GammaPlan 11.5

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