← Back to catalogue

Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Vulnerable patient home alert system FDA UDI
Device Name
ALARM,ADVANTAGE,MAGNETIC TETHER FDA UDI
Model / Reference
MDT5000 FDA UDI
Description
ALARM,ADVANTAGE,MAGNETIC TETHER FDA UDI

Identifiers

Catalog Number
MDT5000 FDA UDI
Primary DI / UDI-DI
00080196750118 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vulnerable patient home alert system

Medline by Medline Industries, Inc. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 11cd122d-3ed5-48bb-a048-ee7ed0b4503c 35 fields · synced May 30, 2026