gudid Primary ID: 38-01-1

Eclipse Probe Cover (UDI 38-01-1)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Eclipse Probe Cover (Model/Catalog Number: 38-01-1) is a medical device manufactured by PARKER LABORATORIES INC. This product is indexed under FDA Product Code / Category Classification IYO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 38-01-1
Product Code / EMDN: IYO
Device Name: A soft disposable ultrasound probe cover
Database Sync Date: 2026-08-09 09:58:58

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 Eclipse Probe Cover?

The registered manufacturer of record for Eclipse Probe Cover is PARKER LABORATORIES INC.

What is the Primary UDI-DI identifier for Eclipse Probe Cover?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 38-01-1.

What classification code is assigned to this device?

This device is registered under product classification code IYO.

Similar Classification Devices (IYO)

Other Devices by PARKER LABORATORIES INC

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