gudid Primary ID: 66142/NA/XL

ORTHOSIS LUMBAR SACRAL W/STANDARD FRONT ALIMED (UDI 66142/NA/XL)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The ORTHOSIS LUMBAR SACRAL W/STANDARD FRONT ALIMED (Model/Catalog Number: 66142/NA/XL) is a medical device manufactured by ALIMED, INC.. This product is indexed under FDA Product Code / Category Classification IPY within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 66142/NA/XL
Product Code / EMDN: IPY
Device Name
Database Sync Date: 2026-08-09 09:17:29

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of ORTHOSIS LUMBAR SACRAL W/STANDARD FRONT ALIMED?

The registered manufacturer of record for ORTHOSIS LUMBAR SACRAL W/STANDARD FRONT ALIMED is ALIMED, INC..

What is the Primary UDI-DI identifier for ORTHOSIS LUMBAR SACRAL W/STANDARD FRONT ALIMED?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 66142/NA/XL.

What classification code is assigned to this device?

This device is registered under product classification code IPY.

Similar Classification Devices (IPY)

Other Devices by ALIMED, INC.

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