HMG

GUDID 10850048235004

Electrode, Electrocardiograph-40 Pouches of 50

Hartman Medical Group LLC

Electrocardiographic electrode, single-use Electrocardiographic electrode, single-use Electrocardiographic electrode, single-use Electrocardiographic electrode, single-use Electrocardiographic electrode, single-use

• Primary Device ID: 10850048235004
• NIH Device Record Key: f9dc4e6b-501d-42c7-9b8f-957897d61a03
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HMG
• Version Model Number: 001
• Company DUNS: 117654675
• Company Name: Hartman Medical Group LLC
• Device Count: 2000
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850048235038 [Unit of Use]
GS1	10850048235004 [Primary]

FDA Product Code

• DRX: Electrode, Electrocardiograph

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: 2023-02-09
• Device Publish Date: 2023-02-01

On-Brand Devices [HMG]

• 10850048235004: Electrode, Electrocardiograph-40 Pouches of 50
• 00850048235007: Electrode, electrocardiograph-Pouch of 50
• 00850048235021: Blood Collection Device-Female Luer Adapter
• 00850048235014: Blood Collection Device-Male Luer Adapter
• 00850048235052: Macro Bore IV extension set with Needle less Y-site and removable needless connector