gudid Primary ID: EXT-3STBNC

NeoConnect Straw (UDI EXT-3STBNC)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The NeoConnect Straw (Model/Catalog Number: EXT-3STBNC) is a medical device manufactured by NEOMED, INC.. This product is indexed under FDA Product Code / Category Classification KNT within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: EXT-3STBNC
Product Code / EMDN: KNT
Device Name: NeoConnect 3" (8 cm) Large Bore Sampling Straw with ENFit Connector, Orange
Database Sync Date: 2026-08-09 09:33:01

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of NeoConnect Straw?

The registered manufacturer of record for NeoConnect Straw is NEOMED, INC..

What is the Primary UDI-DI identifier for NeoConnect Straw?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EXT-3STBNC.

What classification code is assigned to this device?

This device is registered under product classification code KNT.

Similar Classification Devices (KNT)

Other Devices by NEOMED, INC.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint