eudamed_udi
Primary ID: 08592602102128
Retractor MIS left - under sit bone (UDI 08592602102128)
Manufactured by BEZNOSKA, s.r.o.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Retractor MIS left - under sit bone - Primary ID 08592602102128
Device Regulatory Overview
The Retractor MIS left - under sit bone (Model/Catalog Number: 202424) is a medical device manufactured by BEZNOSKA, s.r.o.. This product is indexed under FDA Product Code / Category Classification L0915 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 202424
- Product Code / EMDN
- L0915
- Device Name
- Reusable surgical instruments
- Database Sync Date
- 2026-08-09 16:30:02
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 Retractor MIS left - under sit bone?
The registered manufacturer of record for Retractor MIS left - under sit bone is BEZNOSKA, s.r.o..
What is the Primary UDI-DI identifier for Retractor MIS left - under sit bone?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08592602102128.
What classification code is assigned to this device?
This device is registered under product classification code L0915.
Similar Classification Devices (L0915)
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