eudamed_udi Primary ID: 08591846932478

KPlus 24 cm, size S-M, natural (UDI 08591846932478)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The KPlus 24 cm, size S-M, natural (Model/Catalog Number: LIPO-KP19F03X-N-S-M) is a medical device manufactured by LIPOELASTIC a.s.. This product is indexed under FDA Product Code / Category Classification M030499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: LIPO-KP19F03X-N-S-M
Product Code / EMDN: M030499
Device Name: _/KPlus 24 cm
Database Sync Date: 2026-08-09 16:29:07

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 KPlus 24 cm, size S-M, natural?

The registered manufacturer of record for KPlus 24 cm, size S-M, natural is LIPOELASTIC a.s..

What is the Primary UDI-DI identifier for KPlus 24 cm, size S-M, natural?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08591846932478.

What classification code is assigned to this device?

This device is registered under product classification code M030499.

Similar Classification Devices (M030499)

Other Devices by LIPOELASTIC a.s.

Programmatic Export

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

JSON API Endpoint