Pre-Install Set Helux Pro

GUDID 00887761976450

Pre-Install Set Helux Pro

Baxter Medical Systems GmbH + Co. KG

Medical device service rail
Primary Device ID00887761976450
NIH Device Record Key9909eb38-46b6-477e-aa42-c538e8fa38bc
Commercial Distribution StatusIn Commercial Distribution
Brand NamePre-Install Set Helux Pro
Version Model Number4108051
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
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
GS100887761976450 [Primary]

FDA Product Code

FQPLamp, operating-room

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-03-15
Device Publish Date2023-03-07

Devices Manufactured by Baxter Medical Systems GmbH + Co. KG

00887761943209 - Pads2025-01-28 Pad Carbon Pelvic Extension Set H G U
00887761975682 - Control Units2025-01-28 Footswitch TTH
00887761975699 - Control Units2025-01-28 Footswitch TTH
00887761968554 - Sterilizable Handles2023-07-19 Sterilizable Central Handle, 1 pc
00887761968547 - Sterilizable Handles2023-07-19 Sterilizable Camera Handle, 1 pc
00887761968561 - Sterilizable Handles2023-07-04 Sterilizable ALC Handle, 1 pc
00887761976436 - 4K Refreshing Unit2023-03-15 4K Refreshing Unit
00887761976443 - 4K Camera2023-03-15 4K Camera

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