GUDIDData
eudamed_udi Primary ID: 05055982700726

Flowtron - DVT (UDI 05055982700726)

Manufactured by ArjoHuntleigh AB

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Flowtron - DVT - Primary ID 05055982700726

Device Regulatory Overview

The Flowtron - DVT (Model/Catalog Number: DVT40) is a medical device manufactured by ArjoHuntleigh AB. This product is indexed under FDA Product Code / Category Classification Z120607 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
DVT40
Product Code / EMDN
Z120607
Device Name
Intermittent Pressure Compression Limb Garment
Database Sync Date
2026-08-09 16:28:58

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 Flowtron - DVT?

The registered manufacturer of record for Flowtron - DVT is ArjoHuntleigh AB.

What is the Primary UDI-DI identifier for Flowtron - DVT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05055982700726.

What classification code is assigned to this device?

This device is registered under product classification code Z120607.

Programmatic Export

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

JSON API Endpoint