Philips GoSafe 2 7150MHB

GUDID 00884838084827

7150MHB (GoSafe)

Lifeline Systems Company

Home alert system

• Primary Device ID: 00884838084827
• NIH Device Record Key: dc9e1b79-8dad-43aa-a7b2-832c3335eb6e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Philips GoSafe 2
• Version Model Number: 300000189031
• Catalog Number: 7150MHB
• 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	00884838084827 [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: 2017-10-23

On-Brand Devices [Philips GoSafe 2]

• 00884838084827: 7150MHB (GoSafe)
• 00884838081475: 7150MHB (GoSafe)
• 00884838091573: 7150MHB (GoSafe 2)
• 00884838093638: 7250 (GoSafe 2)