eudamed_udi
Primary ID: 08720256027652
Blade 56 Finisher (UDI 08720256027652)
Manufactured by Spierings Orthopaedics B.V.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Blade 56 Finisher - Primary ID 08720256027652
Device Regulatory Overview
The Blade 56 Finisher (Model/Catalog Number: NCR-1707-56F/RU) is a medical device manufactured by Spierings Orthopaedics B.V.. This product is indexed under FDA Product Code / Category Classification L091101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NCR-1707-56F/RU
- Product Code / EMDN
- L091101
- Device Name
- Noviomagus Cup Resector
- Database Sync Date
- 2026-08-09 16:45:08
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 Blade 56 Finisher?
The registered manufacturer of record for Blade 56 Finisher is Spierings Orthopaedics B.V..
What is the Primary UDI-DI identifier for Blade 56 Finisher?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08720256027652.
What classification code is assigned to this device?
This device is registered under product classification code L091101.
Similar Classification Devices (L091101)
Other Devices by Spierings Orthopaedics B.V.
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