eudamed_udi
Primary ID: 08592602250324
Konos - Cone reamer, D9 (UDI 08592602250324)
Manufactured by BEZNOSKA, s.r.o.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Konos - Cone reamer, D9 - Primary ID 08592602250324
Device Regulatory Overview
The Konos - Cone reamer, D9 (Model/Catalog Number: 400497) is a medical device manufactured by BEZNOSKA, s.r.o.. This product is indexed under FDA Product Code / Category Classification L091102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 400497
- Product Code / EMDN
- L091102
- Device Name
- Reusable surgical instruments
- Database Sync Date
- 2026-08-09 16:29:12
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 Konos - Cone reamer, D9?
The registered manufacturer of record for Konos - Cone reamer, D9 is BEZNOSKA, s.r.o..
What is the Primary UDI-DI identifier for Konos - Cone reamer, D9?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08592602250324.
What classification code is assigned to this device?
This device is registered under product classification code L091102.
Similar Classification Devices (L091102)
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