KBMED (UDI SCB1050)

Manufactured by KB Medical (group), Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The KBMED (Model/Catalog Number: SCB1050) is a medical device manufactured by KB Medical (group), Inc.. This product is indexed under FDA Product Code / Category Classification FQM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: SCB1050
Product Code / EMDN: FQM
Device Name: Cohesive Bandage, Tan, 1"x 5 yard, pack of 60 rolls
Database Sync Date: 2026-08-09 09:09:51

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 KBMED?

The registered manufacturer of record for KBMED is KB Medical (group), Inc..

What is the Primary UDI-DI identifier for KBMED?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SCB1050.

What classification code is assigned to this device?

This device is registered under product classification code FQM.

Similar Classification Devices (FQM)

Other Devices by KB Medical (group), Inc.

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