GKS PRIME FLEX: Trial Insert MOBILE UC/PS Size 7x18mm (UDI 08050323130726)
Manufactured by Permedica S.p.A
Device Regulatory Overview
The GKS PRIME FLEX: Trial Insert MOBILE UC/PS Size 7x18mm (Model/Catalog Number: S52748) is a medical device manufactured by Permedica S.p.A. This product is indexed under FDA Product Code / Category Classification V06010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S52748
- Product Code / EMDN
- V06010102
- Device Name
- Trial Component
- Database Sync Date
- 2026-08-09 16:30:06
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 GKS PRIME FLEX: Trial Insert MOBILE UC/PS Size 7x18mm?
The registered manufacturer of record for GKS PRIME FLEX: Trial Insert MOBILE UC/PS Size 7x18mm is Permedica S.p.A.
What is the Primary UDI-DI identifier for GKS PRIME FLEX: Trial Insert MOBILE UC/PS Size 7x18mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08050323130726.
What classification code is assigned to this device?
This device is registered under product classification code V06010102.
Similar Classification Devices (V06010102)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint