eudamed_udi Primary ID: 04004221058334

pediflex (UDI 04004221058334)

Manufactured by KOB GmbH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The pediflex (Model/Catalog Number: 19933) is a medical device manufactured by KOB GmbH. This product is indexed under FDA Product Code / Category Classification M03030199 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1495-2026 View Full Alert →

MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE, REF NONUNNAS40 KOB article #40307010...

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Technical Specifications

Model Number: 19933
Product Code / EMDN: M03030199
Device Name: 777
Database Sync Date: 2026-08-09 16:46:01

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 pediflex?

The registered manufacturer of record for pediflex is KOB GmbH.

What is the Primary UDI-DI identifier for pediflex?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04004221058334.

What classification code is assigned to this device?

This device is registered under product classification code M03030199.

Similar Classification Devices (M03030199)

Other Devices by KOB GmbH

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