ProSystem: Antirotation Castable Abutment, Internal Hexagon - STANDARD (UDI 08050323034901)
Manufactured by Permedica S.p.A
Device Regulatory Overview
The ProSystem: Antirotation Castable Abutment, Internal Hexagon - STANDARD (Model/Catalog Number: PI410) is a medical device manufactured by Permedica S.p.A. This product is indexed under FDA Product Code / Category Classification Q010280 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PI410
- Product Code / EMDN
- Q010280
- Device Name
- Dental prosthetic component
- Database Sync Date
- 2026-08-09 16:29:11
Full Regulatory Attributes
š 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 ProSystem: Antirotation Castable Abutment, Internal Hexagon - STANDARD?
The registered manufacturer of record for ProSystem: Antirotation Castable Abutment, Internal Hexagon - STANDARD is Permedica S.p.A.
What is the Primary UDI-DI identifier for ProSystem: Antirotation Castable Abutment, Internal Hexagon - STANDARD?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08050323034901.
What classification code is assigned to this device?
This device is registered under product classification code Q010280.
Similar Classification Devices (Q010280)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint