GUDIDData
gudid Primary ID: 0190

Cannula, Adult, Soft Tip w/2` Connector (UDI 0190)

Manufactured by WESTMED, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cannula, Adult, Soft Tip w/2` Connector - Primary ID 0190

Device Regulatory Overview

The Cannula, Adult, Soft Tip w/2` Connector (Model/Catalog Number: 0190) is a medical device manufactured by WESTMED, INC.. This product is indexed under FDA Product Code / Category Classification CAT within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
0190
Product Code / EMDN
CAT
Device Name
Cannula, Adult, Soft Tip w/2` Connector
Database Sync Date
2026-08-09 09:04:13

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 Cannula, Adult, Soft Tip w/2` Connector?

The registered manufacturer of record for Cannula, Adult, Soft Tip w/2` Connector is WESTMED, INC..

What is the Primary UDI-DI identifier for Cannula, Adult, Soft Tip w/2` Connector?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0190.

What classification code is assigned to this device?

This device is registered under product classification code CAT.

Programmatic Export

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

JSON API Endpoint