Philips GoSafe 7100MHB

GUDID 00884838081468

7100MHB (GoSafe)

Lifeline Systems Company

Home alert system

• Primary Device ID: 00884838081468
• NIH Device Record Key: 961b230d-a883-4127-97a8-47995f0f125a
• Commercial Distribution Discontinuation: 2017-10-04
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Philips GoSafe
• Version Model Number: 300000042511
• Catalog Number: 7100MHB
• 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	00884838081468 [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: 2017-10-04

On-Brand Devices [Philips GoSafe]

• 00884838085909: 7000MHB (GoSafe)
• 00884838084810: 7100MHB (GoSafe)
• 00884838081468: 7100MHB (GoSafe)
• 00884838091580: 7100MHB (GoSafe)