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Iq Sensor Alarm With 6 Month Bed Pad System

FDA UDI

Class I (US FDA UDI)

by AliMed, LLC

Identity

Trade Name
IQ SENSOR ALARM WITH 6 MONTH BED PAD SYSTEM FDA UDI
Generic Name
Vulnerable patient home alert system FDA UDI
Model / Reference
70070 FDA UDI

Identifiers

Catalog Number
2970008087 FDA UDI
Primary DI / UDI-DI
00733657227574 FDA UDI
FDA Product Code
KMI FDA UDI
GMDN Term
Vulnerable patient home alert system 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Vulnerable patient home alert system

Iq Sensor Alarm With 6 Month Bed Pad System by AliMed, LLC — Class I — 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

Manufacturer
AliMed, LLC

Sources (1)

  • FDA UDI 47b70709-d82b-42c3-8897-5eeb2f6349d9 34 fields · synced Jun 9, 2026