GUDIDData
gudid Primary ID: M00568480

EndoVive One Step Button (UDI M00568480)

Manufactured by BOSTON SCIENTIFIC CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EndoVive One Step Button - Primary ID M00568480

Device Regulatory Overview

The EndoVive One Step Button (Model/Catalog Number: M00568480) is a medical device manufactured by BOSTON SCIENTIFIC CORPORATION. This product is indexed under FDA Product Code / Category Classification KGC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
M00568480
Product Code / EMDN
KGC
Device Name
Low Profile Percutaneous Endoscopic Gastrostomy Kit
Database Sync Date
2026-08-09 09:41:09

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 EndoVive One Step Button?

The registered manufacturer of record for EndoVive One Step Button is BOSTON SCIENTIFIC CORPORATION.

What is the Primary UDI-DI identifier for EndoVive One Step Button?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M00568480.

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