ENDOPLUS (UDI 08683911189624)
Manufactured by ÖZEL TURKUAZ SAĞLIK HİZMETLERİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ
Device Regulatory Overview
The ENDOPLUS (Model/Catalog Number: 55/06/L31) is a medical device manufactured by ÖZEL TURKUAZ SAĞLIK HİZMETLERİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification Q010507 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 55/06/L31
- Product Code / EMDN
- Q010507
- Device Name
- ENDODONTİK KANAL EĞESİ
- Database Sync Date
- 2026-08-09 16:45:39
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 ENDOPLUS?
The registered manufacturer of record for ENDOPLUS is ÖZEL TURKUAZ SAĞLIK HİZMETLERİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ.
What is the Primary UDI-DI identifier for ENDOPLUS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08683911189624.
What classification code is assigned to this device?
This device is registered under product classification code Q010507.
Similar Classification Devices (Q010507)
Other Devices by ÖZEL TURKUAZ SAĞLIK HİZMETLERİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint