GUDIDData
gudid Primary ID: 000296

Bard Button Replacement Gastrostomy Device (UDI 000296)

Manufactured by Bard Access Systems, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bard Button Replacement Gastrostomy Device - Primary ID 000296

Device Regulatory Overview

The Bard Button Replacement Gastrostomy Device (Model/Catalog Number: 000296) 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
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
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
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
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
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
000296
Product Code / EMDN
KGC
Device Name
24 Fr x 4.4cm Button Kit
Database Sync Date
2026-08-09 10:00:15

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Bard Button Replacement Gastrostomy Device?

The registered manufacturer of record for Bard Button Replacement Gastrostomy Device is Bard Access Systems, Inc..

What is the Primary UDI-DI identifier for Bard Button Replacement Gastrostomy Device?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 000296.

What classification code is assigned to this device?

This device is registered under product classification code KGC.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint