NSCL20795 Custom Med Label Pack NSCL20795

GUDID 20787551040290

NSCL20795 Custom Med Label Pack

XODUS MEDICAL, INC.

Procedural medication labelling set
Primary Device ID20787551040290
NIH Device Record Key35cc7a09-f3c3-4204-9c18-378d52d6bf80
Commercial Distribution StatusIn Commercial Distribution
Brand NameNSCL20795 Custom Med Label Pack
Version Model NumberNSCL20795
Catalog NumberNSCL20795
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 Datetrue
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
GS100787551040296 [Primary]
GS120787551040290 [Package]
Contains: 00787551040296
Package: CASE [100 Units]
In Commercial Distribution

FDA Product Code

LYVLABEL OR TAG, STERILE

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-11-03
Device Publish Date2023-10-26

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