gudid Primary ID: 515

N/A (UDI 515)

Manufactured by Scientific Device Laboratory, Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The N/A (Model/Catalog Number: 515) is a medical device manufactured by Scientific Device Laboratory, Inc.. This product is indexed under FDA Product Code / Category Classification LIB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 515
Product Code / EMDN: LIB
Device Name: Necator americanus Suspension [1cc vial - each]
Database Sync Date: 2026-08-09 09:10:02

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 Scientific Device Laboratory, Inc..

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 515.

What classification code is assigned to this device?

This device is registered under product classification code LIB.

Similar Classification Devices (LIB)

Other Devices by Scientific Device Laboratory, Inc.

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