gudid Primary ID: TT-PPS10-O

KBMED (UDI TT-PPS10-O)

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: TT-PPS10-O) is a medical device manufactured by KB Medical (group), Inc.. This product is indexed under FDA Product Code / Category Classification LXG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: TT-PPS10-O
Product Code / EMDN: LXG
Device Name: TEST TUBE, PP, CAP WITH O-RING PAD, 10ML
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 TT-PPS10-O.

What classification code is assigned to this device?

This device is registered under product classification code LXG.

Similar Classification Devices (LXG)

Other Devices by KB Medical (group), Inc.

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