eudamed_udi
Primary ID: 08050323102167
KONE Stem: Instruments Tray - INOX supp. (UDI 08050323102167)
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 Stem: Instruments Tray - INOX supp. - Primary ID 08050323102167
Device Regulatory Overview
The KONE Stem: Instruments Tray - INOX supp. (Model/Catalog Number: S10701) is a medical device manufactured by Permedica S.p.A. This product is indexed under FDA Product Code / Category Classification S010401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S10701
- Product Code / EMDN
- S010401
- Device Name
- Instruments Tray
- Database Sync Date
- 2026-08-09 16:30:12
Full Regulatory Attributes
π 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 KONE Stem: Instruments Tray - INOX supp.?
The registered manufacturer of record for KONE Stem: Instruments Tray - INOX supp. is Permedica S.p.A.
What is the Primary UDI-DI identifier for KONE Stem: Instruments Tray - INOX supp.?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08050323102167.
What classification code is assigned to this device?
This device is registered under product classification code S010401.
Similar Classification Devices (S010401)
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