GUDIDData
eudamed_udi Primary ID: 08050323152025

GKS PRIME FLEX: Trial Insert TOP AS - Size B-Cx15mm  RIGHT - GREEN (UDI 08050323152025)

Manufactured by Permedica S.p.A

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GKS PRIME FLEX: Trial Insert TOP AS - Size B-Cx15mm  RIGHT - GREEN - Primary ID 08050323152025

Device Regulatory Overview

The GKS PRIME FLEX: Trial Insert TOP AS - Size B-Cx15mm  RIGHT - GREEN (Model/Catalog Number: S53667) 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
S53667
Product Code / EMDN
V06010102
Device Name
Trial Component
Database Sync Date
2026-08-09 16:30:15

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of GKS PRIME FLEX: Trial Insert TOP AS - Size B-Cx15mm  RIGHT - GREEN?

The registered manufacturer of record for GKS PRIME FLEX: Trial Insert TOP AS - Size B-Cx15mm  RIGHT - GREEN is Permedica S.p.A.

What is the Primary UDI-DI identifier for GKS PRIME FLEX: Trial Insert TOP AS - Size B-Cx15mm  RIGHT - GREEN?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08050323152025.

What classification code is assigned to this device?

This device is registered under product classification code V06010102.

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