40666 Pink Pad Air-Assist Trendelenburg + 40666

GUDID 20787551040573

40666 Pink Pad Air-Assist Trendelenburg +

XODUS MEDICAL, INC.

Inflatable patient transfer sliding mattress, single-use
Primary Device ID20787551040573
NIH Device Record Key08765c51-3f71-4681-bc63-2dbaa7a22f35
Commercial Distribution StatusIn Commercial Distribution
Brand Name40666 Pink Pad Air-Assist Trendelenburg +
Version Model Number40666
Catalog Number40666
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
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
GS100787551040579 [Primary]
GS120787551040573 [Package]
Contains: 00787551040579
Package: CASE [3 Units]
In Commercial Distribution

FDA Product Code

FMRDEVICE, TRANSFER, PATIENT, MANUAL

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-04-22
Device Publish Date2024-04-12

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