N/A (UDI 620-08)

Manufactured by Eagle Labs

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

Scannable UDI-DI Representation

Device Regulatory Overview

The N/A (Model/Catalog Number: 620-08) is a medical device manufactured by Eagle Labs. This product is indexed under FDA Product Code / Category Classification HOZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 620-08
Product Code / EMDN: HOZ
Device Name: LASIK shield, 8mm diameter, 6mm edge
Database Sync Date: 2026-08-09 09:09:52

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 N/A?

The registered manufacturer of record for N/A is Eagle Labs.

What is the Primary UDI-DI identifier for N/A?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 620-08.

What classification code is assigned to this device?

This device is registered under product classification code HOZ.

Similar Classification Devices (HOZ)

Other Devices by Eagle Labs

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