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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Basic electric hospital bed FDA UDI
Device Name
ALTERRA MAXX UNIVERSAL BED FDA UDI
Model / Reference
FCEALTMAXX FDA UDI
Description
ALTERRA MAXX UNIVERSAL BED FDA UDI

Identifiers

Catalog Number
FCEALTMAXX FDA UDI
Primary DI / UDI-DI
10888277651838 FDA UDI
FDA Product Code
OSI FDA UDI
GMDN Term
Basic electric hospital bed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5100 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Basic electric hospital bed

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

Similar devices

Also classified as Basic electric hospital bed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1daa02b0-4b09-4315-870c-f45c08731b49 35 fields · synced Jun 8, 2026