eudamed_udi
Primary ID: 08050323165902
GKS PRIME FLEX RK: TRIAL STEM - Ø 10x125mm (UDI 08050323165902)
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 RK: TRIAL STEM - Ø 10x125mm - Primary ID 08050323165902
Device Regulatory Overview
The GKS PRIME FLEX RK: TRIAL STEM - Ø 10x125mm (Model/Catalog Number: S47341) 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
- S47341
- Product Code / EMDN
- V06010102
- Device Name
- Trial Component
- Database Sync Date
- 2026-08-09 16:30:20
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 GKS PRIME FLEX RK: TRIAL STEM - Ø 10x125mm?
The registered manufacturer of record for GKS PRIME FLEX RK: TRIAL STEM - Ø 10x125mm is Permedica S.p.A.
What is the Primary UDI-DI identifier for GKS PRIME FLEX RK: TRIAL STEM - Ø 10x125mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08050323165902.
What classification code is assigned to this device?
This device is registered under product classification code V06010102.
Similar Classification Devices (V06010102)
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