ADVANCED ELECTROCARDIOGRAPH

GUDID B510ECG3F1

ADVANCED INSTRUMENTATIONS, INC.

Electrocardiograph, professional, multichannel Electrocardiograph, professional, multichannel Electrocardiograph, professional, multichannel Electrocardiograph, professional, multichannel Electrocardiograph, professional, multichannel Electrocardiograph, professional, multichannel Electrocardiograph, professional, multichannel Electrocardiograph, professional, multichannel Electrocardiograph, professional, multichannel Electrocardiograph, professional, multichannel

• Primary Device ID: B510ECG3F1
• NIH Device Record Key: 407dcc57-6569-4f41-ad27-054072d52e02
• Commercial Distribution Discontinuation: 2028-04-15
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ADVANCED ELECTROCARDIOGRAPH
• Version Model Number: ECG-3 F
• Company DUNS: 608736880
• Company Name: ADVANCED INSTRUMENTATIONS, INC.
• 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: true
• 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	B510ECG3F1 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K111805

FDA Product Code

• DPS: 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: 2020-04-24
• Device Publish Date: 2020-04-16

On-Brand Devices [ADVANCED ELECTROCARDIOGRAPH]

• B510ECG3PLUS1: ECG-3 PLUS
• B510ECG12C1: ECG-12 C
• B510ECG61: ECG-6
• B510ECG3F1: ECG-3 F
• B510ECG121: ECG-12