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Alimed Ty Sensor, Iq Duo Plus, Connector, Cable C-030r

FDA UDI

Class I (US FDA UDI)

by AliMed, LLC

Identity

Trade Name
ALIMED TY SENSOR, IQ DUO PLUS, CONNECTOR, CABLE C-030R FDA UDI
Generic Name
Vulnerable patient home alert system FDA UDI
Model / Reference
711456 FDA UDI

Identifiers

Catalog Number
2970008753 FDA UDI
Primary DI / UDI-DI
00733657231458 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

Alimed Ty Sensor, Iq Duo Plus, Connector, Cable C-030r 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 79c760b7-2e15-42ed-b767-a311476f6832 34 fields · synced Jun 9, 2026