VITA PHYSIODENS® (UDI J017A62R25T4M0)
Manufactured by VITA Zahnfabrik H. Rauter GmbH & Co. KG
Device Regulatory Overview
The VITA PHYSIODENS® (Model/Catalog Number: A62R25T4M) 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
- A62R25T4M
- Product Code / EMDN
- Q010699
- Device Name
- Artificial teeth
- Database Sync Date
- 2026-08-09 16:28:54
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of VITA PHYSIODENS®?
The registered manufacturer of record for VITA PHYSIODENS® is VITA Zahnfabrik H. Rauter GmbH & Co. KG.
What is the Primary UDI-DI identifier for VITA PHYSIODENS®?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is J017A62R25T4M0.
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
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