SAFE MOBILITY LIGHT KIT,XMIT,PAD,PWR 8' 29148

GUDID 00840828193405

CURBELL MEDICAL PRODUCTS, INC.

Bed/chair occupant movement pressure/vibration sensor
Primary Device ID00840828193405
NIH Device Record Key890c2e08-4767-488a-9603-612a82893128
Commercial Distribution StatusIn Commercial Distribution
Brand NameSAFE MOBILITY LIGHT KIT,XMIT,PAD,PWR 8'
Version Model NumberSML-1000-001118000
Catalog Number29148
Company DUNS796452311
Company NameCURBELL MEDICAL PRODUCTS, INC.
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 Batchtrue
Serial Numberfalse
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

Phone18002357500
Emailmwinter@curbell.com
Phone18002357500
Emailmwinter@curbell.com
Phone18002357500
Emailmwinter@curbell.com
Phone18002357500
Emailmwinter@curbell.com
Phone18002357500
Emailmwinter@curbell.com
Phone18002357500
Emailmwinter@curbell.com
Phone18002357500
Emailmwinter@curbell.com
Phone18002357500
Emailmwinter@curbell.com
Phone18002357500
Emailmwinter@curbell.com
Phone18002357500
Emailmwinter@curbell.com
Phone18002357500
Emailmwinter@curbell.com
Phone18002357500
Emailmwinter@curbell.com
Phone18002357500
Emailmwinter@curbell.com
Phone18002357500
Emailmwinter@curbell.com
Phone18002357500
Emailmwinter@curbell.com
Phone18002357500
Emailmwinter@curbell.com
Phone18002357500
Emailmwinter@curbell.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100840828193405 [Primary]

FDA Product Code

KMIMonitor, Bed Patient

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-11-18
Device Publish Date2024-11-08