HomeSafe AutoAlert Pendant FD100

GUDID 00884838084940

FD100 AutoAlert Button

Lifeline Systems Company

Home alert system

• Primary Device ID: 00884838084940
• NIH Device Record Key: a07ca5fd-312d-432d-8b46-6976053fa26d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HomeSafe AutoAlert Pendant
• Version Model Number: 300000219841
• Catalog Number: FD100
• Company DUNS: 080030042
• Company Name: Lifeline Systems Company
• Device Count: 1
• 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: 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884838084940 [Primary]

FDA Product Code

• ILQ: System, communication, powered

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-05-24

On-Brand Devices [HomeSafe AutoAlert Pendant]

• 00884838087880: FD100 AutoAlert Button
• 00884838085664: FD100 AutoAlert Button
• 00884838084957: FD100 AutoAlert Button
• 00884838084940: FD100 AutoAlert Button
• 00884838081383: FD100 AutoAlert Button
• 00884838071780: FD100 AutoAlert Button
• 00884838071773: FD100 AutoAlert Button
• 00884838071766: FD100 AutoAlert Button
• 00884838099982: FD100 AutoAlert Button