GUDIDData
eudamed_udi Primary ID: 08684531709278

ipekdental (UDI 08684531709278)

Manufactured by İPEKDENT MEDİKAL TIBBİ ALETLER ELEKTRONİK SAN VE TİC LTD ŞTİ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ipekdental - Primary ID 08684531709278

Device Regulatory Overview

The ipekdental (Model/Catalog Number: HK-12-25) is a medical device manufactured by İPEKDENT MEDİKAL TIBBİ ALETLER ELEKTRONİK SAN VE TİC LTD ŞTİ. This product is indexed under FDA Product Code / Category Classification L15900699 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
HK-12-25
Product Code / EMDN
L15900699
Device Name
Non Sterile Dental Hand Tool
Database Sync Date
2026-08-09 16:45:58

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 ipekdental?

The registered manufacturer of record for ipekdental is İPEKDENT MEDİKAL TIBBİ ALETLER ELEKTRONİK SAN VE TİC LTD ŞTİ.

What is the Primary UDI-DI identifier for ipekdental?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08684531709278.

What classification code is assigned to this device?

This device is registered under product classification code L15900699.

Similar Classification Devices (L15900699)

Other Devices by İPEKDENT MEDİKAL TIBBİ ALETLER ELEKTRONİK SAN VE TİC LTD ŞTİ

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