ePatch 2.0 rebuilt

GUDID B146EP2R10

BRAEMAR MANUFACTURING, LLC

Electrocardiographic ambulatory recorder
Primary Device IDB146EP2R10
NIH Device Record Keye0144e3f-4d14-43b4-b155-95f238f95d66
Commercial Distribution StatusIn Commercial Distribution
Brand NameePatch 2.0 rebuilt
Version Model Number02-01997
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
HIBCCB146EP2R10 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DSHRecorder, Magnetic Tape, Medical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-07-21
Device Publish Date2022-07-13

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.