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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Trapeze bar exerciser FDA UDI
Device Name
TRAPEZE,F/ALTERRA BEDS FDA UDI
Model / Reference
FCE1232TPZ FDA UDI
Description
TRAPEZE,F/ALTERRA BEDS FDA UDI

Identifiers

Catalog Number
FCE1232TPZ FDA UDI
Primary DI / UDI-DI
40080196326151 FDA UDI
FDA Product Code
FNL FDA UDI
GMDN Term
Trapeze bar exerciser 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: Trapeze bar exerciser

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

Similar devices

Also classified as Trapeze bar exerciser.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c830dbb7-cbb2-4f6b-826f-95126faa120c 35 fields · synced May 30, 2026