GUDIDData
gudid Primary ID: 12081

WAVE (UDI 12081)

Manufactured by Health Care Logistics, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for WAVE - Primary ID 12081

Device Regulatory Overview

The WAVE (Model/Catalog Number: 12081) is a medical device manufactured by Health Care Logistics, Inc.. This product is indexed under FDA Product Code / Category Classification FXP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
12081
Product Code / EMDN
FXP
Device Name
Shoe Covers, Pack of 10
Database Sync Date
2026-08-09 09:33:17

Full Regulatory Attributes

🔒 Token Gated
{
    "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 WAVE?

The registered manufacturer of record for WAVE is Health Care Logistics, Inc..

What is the Primary UDI-DI identifier for WAVE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 12081.

What classification code is assigned to this device?

This device is registered under product classification code FXP.

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