UNI CHAIR SHORT-TERM-SNAP PAD 29173

GUDID 00840828192132

UNI CHAIR SHORT-TERM-SNAP PAD

CURBELL MEDICAL PRODUCTS, INC.

Bed/chair occupant movement pressure/vibration sensor
Primary Device ID00840828192132
NIH Device Record Key0a988f22-16a1-4c30-a8fd-349278197811
Commercial Distribution StatusIn Commercial Distribution
Brand NameUNI CHAIR SHORT-TERM-SNAP PAD
Version Model NumberCSP-SCP-07
Catalog Number29173
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
GS100840828192132 [Primary]
GS110840828192139 [Package]
Package: Case [10 Units]
In Commercial Distribution

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 Date2024-07-29
Device Publish Date2024-07-19

Devices Manufactured by CURBELL MEDICAL PRODUCTS, INC.

00840828192682 - REGO HUB,HILLROM NAVICARE,NO-NC,NO-P,ALT2024-07-30 REGO HUB,HILLROM NAVICARE,NO-NC,NO-P,ALT
00840828192699 - REGO HUB,ASCOM TELLIGENCE,NO-NC,NO-P2024-07-30 REGO HUB,ASCOM TELLIGENCE,NO-NC,NO-P
00840828192705 - REGO HUB,ASCOM NU,9FT-NO-PWR,RELAYS2024-07-30 REGO HUB,ASCOM NU,9FT-NO-PWR,RELAYS
00840828192712 - UNDER BED LIGHT CONTROLLER ASSEMBLY2024-07-30 UNDER BED LIGHT CONTROLLER ASSEMBLY
00840828192729 - RESPONDER 5, INTERACTIVE2024-07-30 RESPONDER 5, INTERACTIVE
00840828192736 - GEN4 PLUS, DIRECT ACCESS2024-07-30 GEN4 PLUS, DIRECT ACCESS
00840828192743 - GEN4 INTERACTIVE2024-07-30 GEN4 INTERACTIVE
00840828192750 - GEN4 PLUS, RESPONDER 5, ENHANCED2024-07-30 GEN4 PLUS, RESPONDER 5, ENHANCED

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.