NeoLead N301

GUDID 10812594011051

Electrode (Box of 20)

NEOTECH PRODUCTS, INC.

Electrocardiographic electrode, single-use

• Primary Device ID: 10812594011051
• NIH Device Record Key: e238d795-f40c-4277-8d0d-0f2b5163251f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NeoLead
• Version Model Number: 10812594011051
• Catalog Number: N301
• Company DUNS: 198013435
• Company Name: NEOTECH PRODUCTS, INC.
• Device Count: 50
• 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: false
• 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	00812594011047 [Unit of Use]
GS1	10812594011051 [Primary]

FDA Product Code

• DRX: Electrode, Electrocardiograph

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2021-06-14
• Device Publish Date: 2016-09-14

On-Brand Devices [NeoLead]

• 00812594011054: 812594011054
• 10812594011051: Electrode (Box of 20)