DISP NONN COMP SPO2 SNSR,6000CP,PDTR,20" 28799

GUDID 10840828190494

DISP NONIN COMP SPO2 SNSR,6000CP,PDTRC,20”,CLR FLM,NON-STRL,EA

CURBELL MEDICAL PRODUCTS, INC.

Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use
Primary Device ID10840828190494
NIH Device Record Keyaa8f5d0a-09a9-4c40-b0a2-9cd2aee1229a
Commercial Distribution StatusIn Commercial Distribution
Brand NameDISP NONN COMP SPO2 SNSR,6000CP,PDTR,20"
Version Model NumberCSA020DP-P100
Catalog Number28799
Company DUNS796452311
Company NameCURBELL MEDICAL PRODUCTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com
Phone1-800-235-7500
Emailmwinter@curbellmedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100840828190497 [Primary]
GS110840828190494 [Package]
Contains: 00840828190497
Package: Case [24 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DQAOximeter
DSACable, Transducer And Electrode, Patient, (Including Connector)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-11-15
Device Publish Date2023-11-07

Devices Manufactured by CURBELL MEDICAL PRODUCTS, INC.

00840828182294 - REUS,NCLR OXSMRT SPO2 SNSR,9.5',LG CLAM2024-04-18 REUS,NCLR OXSMRT SPO2 SNSR,9.5',LG CLAM
00840828182300 - REUS,NLCR OXSMRT SPO2 SNSR,3.3',LG CLAM2024-04-18 REUS,NLCR OXSMRT SPO2 SNSR,3.3',LG CLAM
00840828182317 - REUS,NLCR OXSMRT SPO2 SNSR,3.3',LG SOFT2024-04-18 REUS,NLCR OXSMRT SPO2 SNSR,3.3',LG SOFT
00840828182324 - REUS,NLCR OXSMRT SPO2 SNSR,3.3',SM SOFT2024-04-18 REUS,NLCR OXSMRT SPO2 SNSR,3.3',SM SOFT
00840828182331 - REUS,NLCR OXMAX SPO2 SNSR,9.5',LG CLAM2024-04-18 REUS,NLCR OXMAX SPO2 SNSR,9.5',LG CLAM
00840828182348 - REUS,NLCR OXMAX SPO2 SNSR,3.3',LG CLAM2024-04-18 REUS,NLCR OXMAX SPO2 SNSR,3.3',LG CLAM
00840828182355 - REUS,NLCR OXMAX SPO2 SNSR,9.5',LG SOFT2024-04-18 REUS,NLCR OXMAX SPO2 SNSR,9.5',LG SOFT
00840828182362 - REUS,NLCR OXMAX SPO2 SNSR,3.3',LG SOFT2024-04-18 REUS,NLCR OXMAX SPO2 SNSR,3.3',LG SOFT
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.