gudid Primary ID: 000356

Bard Button Device Decompression Tube (UDI 000356)

Manufactured by Bard Access Systems, Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Bard Button Device Decompression Tube (Model/Catalog Number: 000356) is a medical device manufactured by Bard Access Systems, Inc.. This product is indexed under FDA Product Code / Category Classification KGC within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2656-2026 View Full Alert →

CK000495APoly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 CK000566Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Cod...

🔒 Compromised Lot & Serial Numbers Locked

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ID: Z-2662-2026 View Full Alert →

CK000727PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138478 CK000729PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code...

🔒 Compromised Lot & Serial Numbers Locked

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ID: Z-2667-2026 View Full Alert →

CK000880Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770 S4153108BDPProvena Midline Catheter 3 Fr Single-Lumen UDI-...

🔒 Compromised Lot & Serial Numbers Locked

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Technical Specifications

Model Number: 000356
Product Code / EMDN: KGC
Device Name: Button Decompression Tube
Database Sync Date: 2026-08-09 09:52:56

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 Bard Button Device Decompression Tube?

The registered manufacturer of record for Bard Button Device Decompression Tube is Bard Access Systems, Inc..

What is the Primary UDI-DI identifier for Bard Button Device Decompression Tube?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 000356.

What classification code is assigned to this device?

This device is registered under product classification code KGC.

Similar Classification Devices (KGC)

Other Devices by Bard Access Systems, Inc.

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