GUDIDData
eudamed_udi Primary ID: 30734000675746

PharmaFlex Direct Swivel Port (UDI 30734000675746)

Manufactured by Pharma Systems AB

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PharmaFlex Direct Swivel Port - Primary ID 30734000675746

Device Regulatory Overview

The PharmaFlex Direct Swivel Port (Model/Catalog Number: 5003s) is a medical device manufactured by Pharma Systems AB. This product is indexed under FDA Product Code / Category Classification R020299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
5003s
Product Code / EMDN
R020299
Device Name
Catheter Mounts and Elbows
Database Sync Date
2026-08-09 17:41:27

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 PharmaFlex Direct Swivel Port?

The registered manufacturer of record for PharmaFlex Direct Swivel Port is Pharma Systems AB.

What is the Primary UDI-DI identifier for PharmaFlex Direct Swivel Port?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 30734000675746.

What classification code is assigned to this device?

This device is registered under product classification code R020299.

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