GUDIDData
eudamed_udi Primary ID: 08682704632576

Distalock Femur End Cap 20mm Extension (UDI 08682704632576)

Manufactured by OTTA TIBBİ CİHAZLAR VE MEDİKAL A.Ş.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Distalock Femur End Cap 20mm Extension - Primary ID 08682704632576

Device Regulatory Overview

The Distalock Femur End Cap 20mm Extension (Model/Catalog Number: 220-000-020) is a medical device manufactured by OTTA TIBBİ CİHAZLAR VE MEDİKAL A.Ş.. This product is indexed under FDA Product Code / Category Classification P091280 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
220-000-020
Product Code / EMDN
P091280
Device Name
Distalock Femur End Cap 20mm Extension
Database Sync Date
2026-08-09 16:28:58

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Distalock Femur End Cap 20mm Extension?

The registered manufacturer of record for Distalock Femur End Cap 20mm Extension is OTTA TIBBİ CİHAZLAR VE MEDİKAL A.Ş..

What is the Primary UDI-DI identifier for Distalock Femur End Cap 20mm Extension?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682704632576.

What classification code is assigned to this device?

This device is registered under product classification code P091280.

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