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Leg & Foot Elevator

FDA UDI

Class I (US FDA UDI)

by Primo Inc

Identity

Trade Name
Leg & Foot Elevator FDA UDI
Generic Name
Freestanding patient positioner, single-use FDA UDI
Device Name
Leg & Foot Elevator -Short (27.5"L x 14.75"W x 8.5"H) FDA UDI
Model / Reference
LFE01S FDA UDI
Description
Leg & Foot Elevator -Short (27.5"L x 14.75"W x 8.5"H) FDA UDI

Identifiers

Catalog Number
LFE01S FDA UDI
Primary DI / UDI-DI
00810006682113 FDA UDI
FDA Product Code
FMP FDA UDI
GMDN Term
Freestanding patient positioner, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6450 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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: Freestanding patient positioner, single-use

Leg & Foot Elevator by Primo Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Freestanding patient positioner, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Primo Inc

Sources (1)

  • FDA UDI 4979cb0e-3efb-4192-8af7-1804beea1b4a 34 fields · synced May 30, 2026