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Senior Living Alert Device AutoAlert with Indicator

FDA UDI

Class II (US FDA UDI)

by Lifeline Systems, Inc.

Identity

Trade Name
Senior Living Alert Device AutoAlert with Indicator FDA UDI
Generic Name
Vulnerable patient home alert system FDA UDI
Device Name
7000AHB AutoAlert Button Senior Living FDA UDI
Model / Reference
300000350661 FDA UDI
Description
7000AHB AutoAlert Button Senior Living FDA UDI

Identifiers

Catalog Number
7000AHB-SL FDA UDI
Primary DI / UDI-DI
00884838085794 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
Not 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

Senior Living Alert Device AutoAlert with Indicator by Lifeline Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lifeline Systems, Inc.

Sources (1)

  • FDA UDI 9ad86ae3-0336-4dd6-aa4c-1242bce27958 35 fields · synced Jun 1, 2026