GUDIDData
gudid Primary ID: 445445

Onclarity Self-Collection Kit-Viper LT (UDI 445445)

Manufactured by BECTON, DICKINSON AND COMPANY

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Onclarity Self-Collection Kit-Viper LT - Primary ID 445445

Device Regulatory Overview

The Onclarity Self-Collection Kit-Viper LT (Model/Catalog Number: 445445) is a medical device manufactured by BECTON, DICKINSON AND COMPANY. This product is indexed under FDA Product Code / Category Classification SEP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
445445
Product Code / EMDN
SEP
Device Name
Onclarity Self-Collection Kit-Viper LT
Database Sync Date
2026-08-09 10:02:46

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 Onclarity Self-Collection Kit-Viper LT?

The registered manufacturer of record for Onclarity Self-Collection Kit-Viper LT is BECTON, DICKINSON AND COMPANY.

What is the Primary UDI-DI identifier for Onclarity Self-Collection Kit-Viper LT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 445445.

What classification code is assigned to this device?

This device is registered under product classification code SEP.

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