eudamed_udi Primary ID: 08699041095575

KARAOĞLU (UDI 08699041095575)

Manufactured by KARAOĞLU BASKÜL VE CERRAHİ ALETLER İMAL. SAN. TİC. LTD. ŞTİ

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The KARAOĞLU (Model/Catalog Number: KZ315.10) is a medical device manufactured by KARAOĞLU BASKÜL VE CERRAHİ ALETLER İMAL. SAN. TİC. LTD. ŞTİ. This product is indexed under FDA Product Code / Category Classification L01040503 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: KZ315.10
Product Code / EMDN: L01040503
Device Name: CUTTERS
Database Sync Date: 2026-08-09 16:28:44

Full Regulatory Attributes

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{
    "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 KARAOĞLU?

The registered manufacturer of record for KARAOĞLU is KARAOĞLU BASKÜL VE CERRAHİ ALETLER İMAL. SAN. TİC. LTD. ŞTİ.

What is the Primary UDI-DI identifier for KARAOĞLU?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08699041095575.

What classification code is assigned to this device?

This device is registered under product classification code L01040503.

Similar Classification Devices (L01040503)

Other Devices by KARAOĞLU BASKÜL VE CERRAHİ ALETLER İMAL. SAN. TİC. LTD. ŞTİ

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