eudamed_udi
Primary ID: 08050323053254
KONE Trial STEM 12/14 - Size 21 (UDI 08050323053254)
Manufactured by Permedica S.p.A
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KONE Trial STEM 12/14 - Size 21 - Primary ID 08050323053254
Device Regulatory Overview
The KONE Trial STEM 12/14 - Size 21 (Model/Catalog Number: S10721) is a medical device manufactured by Permedica S.p.A. This product is indexed under FDA Product Code / Category Classification V06010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S10721
- Product Code / EMDN
- V06010101
- Device Name
- Trial Component
- Database Sync Date
- 2026-08-09 16:47:59
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 KONE Trial STEM 12/14 - Size 21?
The registered manufacturer of record for KONE Trial STEM 12/14 - Size 21 is Permedica S.p.A.
What is the Primary UDI-DI identifier for KONE Trial STEM 12/14 - Size 21?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08050323053254.
What classification code is assigned to this device?
This device is registered under product classification code V06010101.
Similar Classification Devices (V06010101)
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