gudid Primary ID: Nitrile PF Exam PLUS 5.0 (Bull) L

Ventyv (UDI Nitrile PF Exam PLUS 5.0 (Bull) L)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Ventyv (Model/Catalog Number: Nitrile PF Exam PLUS 5.0 (Bull) L) is a medical device manufactured by SRI TRANG USA, INC.. This product is indexed under FDA Product Code / Category Classification QDO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Nitrile PF Exam PLUS 5.0 (Bull) L
Product Code / EMDN: QDO
Device Name
Database Sync Date: 2026-08-09 09:13:49

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 Ventyv?

The registered manufacturer of record for Ventyv is SRI TRANG USA, INC..

What is the Primary UDI-DI identifier for Ventyv?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Nitrile PF Exam PLUS 5.0 (Bull) L.

What classification code is assigned to this device?

This device is registered under product classification code QDO.

Similar Classification Devices (QDO)

Other Devices by SRI TRANG USA, INC.

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