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Slimline Personal Help Wriststrap

FDA UDI

Class II (US FDA UDI)

by Lifeline Systems, Inc.

Identity

Trade Name
Slimline Personal Help Wriststrap FDA UDI
Generic Name
Vulnerable patient home alert system FDA UDI
Device Name
SL318G Personal Help Button/Neckcord FDA UDI
Model / Reference
1840440 FDA UDI
Description
SL318G Personal Help Button/Neckcord FDA UDI

Identifiers

Catalog Number
SL318G FDA UDI
Primary DI / UDI-DI
00884838071841 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Vulnerable patient home alert system

Slimline Personal Help Wriststrap 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 b057628c-b007-4ad3-a022-932707e82f44 34 fields · synced Jun 1, 2026