DURADENT - ML B1 98X25 - SAPPHIRE ZİRKON BLOK (UDI 08699197582820)
Manufactured by ERK DENTAL MED. TIBBİ. MALZ. TUR. SAN. VE TİC. LTD. ŞTİ.
Device Regulatory Overview
The DURADENT - ML B1 98X25 - SAPPHIRE ZİRKON BLOK (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
- SAPPHIRE ZİRKON BLOK
- Database Sync Date
- 2026-08-09 16:28:44
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 DURADENT - ML B1 98X25 - SAPPHIRE ZİRKON BLOK?
The registered manufacturer of record for DURADENT - ML B1 98X25 - SAPPHIRE ZİRKON BLOK is ERK DENTAL MED. TIBBİ. MALZ. TUR. SAN. VE TİC. LTD. ŞTİ..
What is the Primary UDI-DI identifier for DURADENT - ML B1 98X25 - SAPPHIRE ZİRKON BLOK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08699197582820.
What classification code is assigned to this device?
This device is registered under product classification code Q010699.
Similar Classification Devices (Q010699)
Other Devices by ERK DENTAL MED. TIBBİ. MALZ. TUR. SAN. VE TİC. LTD. ŞTİ.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint