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HomeSafe Standard Home Communicator

FDA UDI

Class II (US FDA UDI)

by Lifeline Systems, Inc.

Identity

Trade Name
HomeSafe Standard Home Communicator FDA UDI
Generic Name
Vulnerable patient home alert system FDA UDI
Device Name
6800AT Refurbished Home Communicator FDA UDI
Model / Reference
1840551 FDA UDI
Description
6800AT Refurbished Home Communicator FDA UDI

Identifiers

Catalog Number
6800AT FDA UDI
Primary DI / UDI-DI
00884838071582 FDA UDI
FDA Product Code
ILQ FDA UDI
GMDN Term
Vulnerable patient home alert system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3710 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Vulnerable patient home alert system

HomeSafe Standard Home Communicator by Lifeline Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vulnerable patient home alert system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4479b5b6-0f8b-419a-9b67-2ed84c45b910 34 fields · synced May 30, 2026