eudamed_udi Primary ID: 04004221064113

KREWI-Lastic S (UDI 04004221064113)

Manufactured by KOB GmbH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The KREWI-Lastic S (Model/Catalog Number: 540106) is a medical device manufactured by KOB GmbH. This product is indexed under FDA Product Code / Category Classification M0304010102 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: 540106
Product Code / EMDN: M0304010102
Device Name: 530
Database Sync Date: 2026-08-09 16:49:25

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 KREWI-Lastic S?

The registered manufacturer of record for KREWI-Lastic S is KOB GmbH.

What is the Primary UDI-DI identifier for KREWI-Lastic S?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04004221064113.

What classification code is assigned to this device?

This device is registered under product classification code M0304010102.

Similar Classification Devices (M0304010102)

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