TS 7500

GUDID 00887761974326

TruSystem 7500 Hybrid (MC)

TRUMPF Medizin Systeme GmbH + Co. KG

Electromechanical operating table base
Primary Device ID00887761974326
NIH Device Record Keyebe7e81c-1347-43bd-83f5-1b7affb59bfc
Commercial Distribution StatusIn Commercial Distribution
Brand NameTS 7500
Version Model Number1773204
Company DUNS330961223
Company NameTRUMPF Medizin Systeme 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

Device Identifiers

Device Issuing AgencyDevice ID
GS100887761974326 [Primary]

FDA Product Code

KXJTable, radiologic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-01-13
Device Publish Date2023-01-05

On-Brand Devices [TS 7500]

00887761974494Operating table top SQ14 X-TRA UT
00887761974456OR table top Carbon FL U V
00887761974340Operating table top PTS Combi Suite U
00887761974326TruSystem 7500 Hybrid (MC)
00887761974098OR table top Carbon X-TRA 7500 U V
00887761974081TruSystem 7500 Hybrid (FC)
00887761974074TruSystem 7500 Hybrid (SC)
00887761974067TruSystem 7500 Hybrid Plus (FC)
00887761974050TruSystem 7500 Hybrid Plus (SC)

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