GKS BUTTERFLY: ROTATING TRIAL TIBIA v2 - Medium LEFT (UDI 08050323165568)
Manufactured by Permedica S.p.A
Device Regulatory Overview
The GKS BUTTERFLY: ROTATING TRIAL TIBIA v2 - Medium LEFT (Model/Catalog Number: S40524) 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
- S40524
- Product Code / EMDN
- V06010102
- Device Name
- Trial Component
- Database Sync Date
- 2026-08-09 16:46:04
Full Regulatory Attributes
š Token Gated
{
"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 BUTTERFLY: ROTATING TRIAL TIBIA v2 - Medium LEFT?
The registered manufacturer of record for GKS BUTTERFLY: ROTATING TRIAL TIBIA v2 - Medium LEFT is Permedica S.p.A.
What is the Primary UDI-DI identifier for GKS BUTTERFLY: ROTATING TRIAL TIBIA v2 - Medium LEFT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08050323165568.
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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