SPK11602 ProAxis Table Kit SPK11602

GUDID 20787551041082

SPK11602 ProAxis Table Kit

XODUS MEDICAL, INC.

Operating table patient positioning set, single-use
Primary Device ID20787551041082
NIH Device Record Keyd99a12d7-5603-4c70-acff-76606cdc38c1
Commercial Distribution StatusIn Commercial Distribution
Brand NameSPK11602 ProAxis Table Kit
Version Model NumberSPK11602
Catalog NumberSPK11602
Company DUNS868042664
Company NameXODUS MEDICAL, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(724)337-5500
Emailplloyd@xodusmedical.com
Phone+1(724)337-5500
Emailplloyd@xodusmedical.com
Phone+1(724)337-5500
Emailplloyd@xodusmedical.com
Phone+1(724)337-5500
Emailplloyd@xodusmedical.com
Phone+1(724)337-5500
Emailplloyd@xodusmedical.com
Phone+1(724)337-5500
Emailplloyd@xodusmedical.com
Phone+1(724)337-5500
Emailplloyd@xodusmedical.com
Phone+1(724)337-5500
Emailplloyd@xodusmedical.com
Phone+1(724)337-5500
Emailplloyd@xodusmedical.com
Phone+1(724)337-5500
Emailplloyd@xodusmedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100787551041088 [Primary]
GS120787551041082 [Package]
Contains: 00787551041088
Package: CASE [6 Units]
In Commercial Distribution

FDA Product Code

CCXSUPPORT, PATIENT POSITION

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-04-24
Device Publish Date2025-04-16

Devices Manufactured by XODUS MEDICAL, INC.

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20787551041143 - CL25296 Custom Med Label Pack2025-04-24 CL25296 Custom Med Label Pack
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