iBEAM®

GUDID 04056719002213

iBEAM® one Couchtop is intended to support the patient during radiation therapy or radiation therapy simulation.

Medical Intelligence Medizintechnik GmbH

Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered Accelerator system table, non-powered
Primary Device ID04056719002213
NIH Device Record Keye42c2243-89f2-4951-a9ef-a587f77a9b9a
Commercial Distribution StatusIn Commercial Distribution
Brand NameiBEAM®
Version Model NumberP10105-300
Company DUNS314546664
Company NameMedical Intelligence Medizintechnik GmbH
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
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

Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com
Phone+1(855)693-5358
Emailinfo@elekta.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104056719002213 [Primary]

FDA Product Code

IXQTable, radiographic, stationary top

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-08-28
Device Publish Date2020-08-20

On-Brand Devices [iBEAM®]

04056719002237iBEAM evo CT Overlay RT is intended to support the patient during CT and PET CT imaging procedur
04056719002213iBEAM® one Couchtop is intended to support the patient during radiation therapy or radiation th

Trademark Results [iBEAM]

Mark Image

Registration | Serial
Company
Trademark
Application Date
IBEAM
IBEAM
97357862 not registered Live/Pending
STOCKTON PRODUCTS
2022-04-11
IBEAM
IBEAM
97349680 not registered Live/Pending
STOCKTON PRODUCTS
2022-04-06
IBEAM
IBEAM
90757406 not registered Live/Pending
BEAM Society Limited
2021-06-06
IBEAM
IBEAM
87330337 not registered Live/Pending
Tau Delta Holdings, Inc.
2017-02-09
IBEAM
IBEAM
85482208 not registered Dead/Abandoned
Aios Technology Limited
2011-11-29
IBEAM
IBEAM
85293555 4192788 Live/Registered
Consolidated Asset Recovery Systems, Inc.
2011-04-13
IBEAM
IBEAM
85133883 not registered Dead/Abandoned
Modernfold, Inc.
2010-09-20
IBEAM
IBEAM
78593746 3262414 Dead/Cancelled
SHARPER IMAGE HOLDINGS LLC
2005-03-23
IBEAM
IBEAM
78352534 2987332 Dead/Cancelled
IBEAM GROUP, LLC
2004-01-15
IBEAM
IBEAM
78105339 not registered Dead/Abandoned
McKay, Christopher, B.
2002-01-29
IBEAM
IBEAM
78002707 not registered Dead/Abandoned
LaserMax, Inc.
2000-04-05
IBEAM
IBEAM
77598339 not registered Dead/Abandoned
L.R. BAGGS CORPORATION
2008-10-22

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.