GUDIDData
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gudid Primary ID: 3813-875-000-9

SuperClear (UDI 3813-875-000-9)

Manufactured by Labcon

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SuperClear - Primary ID 3813-875-000-9

Device Regulatory Overview

The SuperClear (Model/Catalog Number: 3813-875-000-9) is a medical device manufactured by Labcon. This product is indexed under FDA Product Code / Category Classification KDT within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
3813-875-000-9
Product Code / EMDN
KDT
Device Name
SuperClear 5mL Specimen Collection and Transport Tubes, Bulk, Sterile, Tubes Only
Database Sync Date
2026-08-09 09:23:10

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 SuperClear?

The registered manufacturer of record for SuperClear is Labcon.

What is the Primary UDI-DI identifier for SuperClear?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3813-875-000-9.

What classification code is assigned to this device?

This device is registered under product classification code KDT.

Similar Classification Devices (KDT)

Other Devices by Labcon

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