GUDIDData
gudid Primary ID: 2015-0090

ACCURUN (UDI 2015-0090)

Manufactured by Lgc Clinical Diagnostics, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ACCURUN - Primary ID 2015-0090

Device Regulatory Overview

The ACCURUN (Model/Catalog Number: 2015-0090) is a medical device manufactured by Lgc Clinical Diagnostics, Inc.. This product is indexed under FDA Product Code / Category Classification KSF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
2015-0090
Product Code / EMDN
KSF
Device Name
ACCURUN 155 Series 2000 Anti-Treponema (Syphilis) 3 x 2.0 mL
Database Sync Date
2026-08-09 09:31:28

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 ACCURUN?

The registered manufacturer of record for ACCURUN is Lgc Clinical Diagnostics, Inc..

What is the Primary UDI-DI identifier for ACCURUN?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2015-0090.

What classification code is assigned to this device?

This device is registered under product classification code KSF.

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