GUDIDData
gudid Primary ID: 5540

5540 7L SYRINGE (UDI 5540)

Manufactured by HANS RUDOLPH, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 5540 7L SYRINGE - Primary ID 5540

Device Regulatory Overview

The 5540 7L SYRINGE (Model/Catalog Number: 5540) is a medical device manufactured by HANS RUDOLPH, INC.. This product is indexed under FDA Product Code / Category Classification BXW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
5540
Product Code / EMDN
BXW
Device Name
SERIES 5540 1/4-28 THD OUTLET"
Database Sync Date
2026-08-09 09:31:22

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 5540 7L SYRINGE?

The registered manufacturer of record for 5540 7L SYRINGE is HANS RUDOLPH, INC..

What is the Primary UDI-DI identifier for 5540 7L SYRINGE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5540.

What classification code is assigned to this device?

This device is registered under product classification code BXW.

Programmatic Export

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

JSON API Endpoint