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Securitas Healthcare

FDA UDI

Class I (US FDA UDI)

by Securitas Healthcare LLC

Identity

Trade Name
Securitas Healthcare FDA UDI
Generic Name
Ambulatory fall sensor FDA UDI
Device Name
BED PAD, 3.5x29, 90-DAY, 8FT (Hardshell) FDA UDI
Model / Reference
74011 FDA UDI
Description
BED PAD, 3.5x29, 90-DAY, 8FT (Hardshell) FDA UDI

Identifiers

Catalog Number
74011 FDA UDI
Primary DI / UDI-DI
00840948103322 FDA UDI
FDA Product Code
KMI FDA UDI
GMDN Term
Ambulatory fall sensor FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.2400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

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: Ambulatory fall sensor

Securitas Healthcare by Securitas Healthcare LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ambulatory fall sensor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Securitas Healthcare LLC

Sources (1)

  • FDA UDI 0ade7185-f4bf-457e-ab66-ba114f3a85e5 34 fields · synced May 30, 2026