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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Bed/chair occupant movement pressure/vibration sensor FDA UDI
Device Name
ALARM CORD,W/CLIPS, F/MDT5000(Z), 3/BG FDA UDI
Model / Reference
MDT5000XCD FDA UDI
Description
ALARM CORD,W/CLIPS, F/MDT5000(Z), 3/BG FDA UDI

Identifiers

Catalog Number
MDT5000XCD FDA UDI
Primary DI / UDI-DI
10080196373239 FDA UDI
FDA Product Code
KMI FDA UDI
GMDN Term
Bed/chair occupant movement pressure/vibration 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

No

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

No

FDA UDI

Category: Bed/chair occupant movement pressure/vibration sensor

Medline by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bed/chair occupant movement pressure/vibration sensor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI a3009465-b9c6-42ae-8ae1-4404a7c0e9fa 35 fields · synced May 29, 2026