GUDIDData
eudamed_udi Primary ID: 08684041341678

DURADENT - ML AT BL3 - EVEREST ZİRKON BLOK - (98x20) (UDI 08684041341678)

Manufactured by ERK DENTAL MED. TIBBİ. MALZ. TUR. SAN. VE TİC. LTD. ŞTİ.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DURADENT - ML AT BL3 - EVEREST ZİRKON BLOK - (98x20) - Primary ID 08684041341678

Device Regulatory Overview

The DURADENT - ML AT BL3 - EVEREST ZİRKON BLOK - (98x20) (Model/Catalog Number: YOK) is a medical device manufactured by ERK DENTAL MED. TIBBİ. MALZ. TUR. SAN. VE TİC. LTD. ŞTİ.. This product is indexed under FDA Product Code / Category Classification Q010699 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
YOK
Product Code / EMDN
Q010699
Device Name
EVEREST ZİRKON BLOK - (98x20)
Database Sync Date
2026-08-09 16:28:46

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 DURADENT - ML AT BL3 - EVEREST ZİRKON BLOK - (98x20)?

The registered manufacturer of record for DURADENT - ML AT BL3 - EVEREST ZİRKON BLOK - (98x20) is ERK DENTAL MED. TIBBİ. MALZ. TUR. SAN. VE TİC. LTD. ŞTİ..

What is the Primary UDI-DI identifier for DURADENT - ML AT BL3 - EVEREST ZİRKON BLOK - (98x20)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08684041341678.

What classification code is assigned to this device?

This device is registered under product classification code Q010699.

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