GUDIDData
eudamed_udi Primary ID: 04260157728264

Unspecified Brand (UDI 04260157728264)

Manufactured by Allmed Medical GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 04260157728264

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: KS815/816/BVS/N) is a medical device manufactured by Allmed Medical GmbH. This product is indexed under FDA Product Code / Category Classification F020199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
KS815/816/BVS/N
Product Code / EMDN
F020199
Device Name
Arterial and Venous Bloodline
Database Sync Date
2026-08-09 16:28:46

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is Allmed Medical GmbH.

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260157728264.

What classification code is assigned to this device?

This device is registered under product classification code F020199.

Programmatic Export

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

JSON API Endpoint