ePatch 2.0 rebuilt

GUDID B146EP2R10

BRAEMAR MANUFACTURING, LLC

Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder Electrocardiographic ambulatory recorder

• Primary Device ID: B146EP2R10
• NIH Device Record Key: e0144e3f-4d14-43b4-b155-95f238f95d66
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ePatch 2.0 rebuilt
• Version Model Number: 02-01997
• Company DUNS: 049529118
• Company Name: BRAEMAR MANUFACTURING, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B146EP2R10 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K171410

FDA Product Code

• DSH: Recorder, Magnetic Tape, Medical

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-07-21
• Device Publish Date: 2022-07-13

Devices Manufactured by BRAEMAR MANUFACTURING, LLC

• B146C6M20 - C6 Monitor UGW: 2023-12-14
• B146EP2510 - ePatch 2.5, BTH: 2023-12-13
• B146EP2520 - ePatch 2.5, BTI: 2023-11-30
• B146C6M60 - C6 Monitor A10e, Sprint: 2023-06-23
• B146C6M80 - C6 Monitor A13, T Mobile: 2023-06-23
• B146C6M90 - C6 Monitor A13, Verizon: 2023-06-23
• B146EP2R10 - ePatch 2.0 rebuilt: 2022-07-21
• B146EP2R10 - ePatch 2.0 rebuilt: 2022-07-21
• B146EPE1 - ePatch Electrode-patch: 2022-04-08