GUDIDData
eudamed_udi Primary ID: 08682022062215

ONECARE (UDI 08682022062215)

Manufactured by KAF GRUP SAĞLIK HİZMETLERİ İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ONECARE - Primary ID 08682022062215

Device Regulatory Overview

The ONECARE (Model/Catalog Number: KAFG02) is a medical device manufactured by KAF GRUP SAĞLIK HİZMETLERİ İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification T99 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
KAFG02
Product Code / EMDN
T99
Device Name
BARRIER CREAM INCONTINANCE PERINEAL CLOTHS
Database Sync Date
2026-08-09 16:46:10

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 ONECARE?

The registered manufacturer of record for ONECARE is KAF GRUP SAĞLIK HİZMETLERİ İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ.

What is the Primary UDI-DI identifier for ONECARE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682022062215.

What classification code is assigned to this device?

This device is registered under product classification code T99.

Programmatic Export

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

JSON API Endpoint