VITA VMK Master® (UDI J017B48069120)
Manufactured by VITA Zahnfabrik H. Rauter GmbH & Co. KG
Device Regulatory Overview
The VITA VMK Master® (Model/Catalog Number: B4806912) is a medical device manufactured by VITA Zahnfabrik H. Rauter GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification Q010699 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- B4806912
- Product Code / EMDN
- Q010699
- Device Name
- Veneering Ceramic
- Database Sync Date
- 2026-08-09 16:28:56
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 VITA VMK Master®?
The registered manufacturer of record for VITA VMK Master® is VITA Zahnfabrik H. Rauter GmbH & Co. KG.
What is the Primary UDI-DI identifier for VITA VMK Master®?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is J017B48069120.
What classification code is assigned to this device?
This device is registered under product classification code Q010699.
Similar Classification Devices (Q010699)
Other Devices by VITA Zahnfabrik H. Rauter GmbH & Co. KG
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint