GUDIDData
eudamed_udi Primary ID: 08680395401549

119 M (UDI 08680395401549)

Manufactured by AURAFİX HEALTH PRODUCTS DIŞ TİCARET VE SANAYİ ANONİM ŞİRKETİ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 119 M - Primary ID 08680395401549

Device Regulatory Overview

The 119 M (Model/Catalog Number: 119 M) is a medical device manufactured by AURAFİX HEALTH PRODUCTS DIŞ TİCARET VE SANAYİ ANONİM ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification Y061209 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
119 M
Product Code / EMDN
Y061209
Device Name
ORTHOPEDIC KNEE SUPPORTS
Database Sync Date
2026-08-09 16:30:10

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 119 M?

The registered manufacturer of record for 119 M is AURAFİX HEALTH PRODUCTS DIŞ TİCARET VE SANAYİ ANONİM ŞİRKETİ.

What is the Primary UDI-DI identifier for 119 M?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08680395401549.

What classification code is assigned to this device?

This device is registered under product classification code Y061209.

Similar Classification Devices (Y061209)

Other Devices by AURAFİX HEALTH PRODUCTS DIŞ TİCARET VE SANAYİ ANONİM ŞİRKETİ

Programmatic Export

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

JSON API Endpoint