BTP-1000LW

GUDID B146ELWA10

BRAEMAR MANUFACTURING, LLC

Electrocardiographic ambulatory recorder
Primary Device IDB146ELWA10
NIH Device Record Key6edecbcb-537c-4956-8d3b-7413d1ee6c82
Commercial Distribution StatusIn Commercial Distribution
Brand NameBTP-1000LW
Version Model Number02-00124
Company DUNS049529118
Company NameBRAEMAR MANUFACTURING, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB146ELWA10 [Primary]

FDA Product Code

DSIDetector And Alarm, Arrhythmia
IKDCable, Electrode

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-07-23
Device Publish Date2020-07-15

Devices Manufactured by BRAEMAR MANUFACTURING, LLC

B146C6R30 - C6 Sensor 3.0, Rebuilt2024-07-04
B146EP25R0 - ePatch Sensor 2.5, Rebuilt2024-07-04
B146C6M20 - C6 Monitor UGW2023-12-14
B146EP2510 - ePatch 2.5, BTH2023-12-13
B146EP2520 - ePatch 2.5, BTI2023-11-30
B146C6M60 - C6 Monitor A10e, Sprint2023-06-23
B146C6M80 - C6 Monitor A13, T Mobile2023-06-23
B146C6M90 - C6 Monitor A13, Verizon2023-06-23

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