Pre-Install Set

GUDID 00887761968134

Pre-Install Set TruLight 5000 / 3000

Baxter Medical Systems GmbH + Co. KG

Medical device service rail
Primary Device ID00887761968134
NIH Device Record Key98e84f0b-8d98-424a-a21c-4e5a14b3f212
Commercial Distribution StatusIn Commercial Distribution
Brand NamePre-Install Set
Version Model Number4038051
Company DUNS330961223
Company NameBaxter Medical Systems GmbH + Co. KG
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 Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS100887761968134 [Primary]

FDA Product Code

FTDLamp, surgical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2023-02-09
Device Publish Date2022-12-15

On-Brand Devices [Pre-Install Set]

00887761968196Pre-Install Set VidiaPort
00887761968134Pre-Install Set TruLight 5000 / 3000
00887761968127Pre-Install Set iLED 7

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