gudid Primary ID: PROBE COVER-LATEX FREE

ECLIPSE (UDI PROBE COVER-LATEX FREE)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ECLIPSE (Model/Catalog Number: PROBE COVER-LATEX FREE) 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: PROBE COVER-LATEX FREE
Product Code / EMDN: IYO
Device Name: Eclipse Probe Cover-latex free, 64 mm / 44 x 241 mm
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?

The registered manufacturer of record for ECLIPSE is PARKER LABORATORIES INC.

What is the Primary UDI-DI identifier for ECLIPSE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PROBE COVER-LATEX FREE.

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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