eudamed_udi
Primary ID: 04251406607683
MKS Osteo flex - reduced height large size 5 (UDI 04251406607683)
Manufactured by albrecht GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MKS Osteo flex - reduced height large size 5 - Primary ID 04251406607683
Device Regulatory Overview
The MKS Osteo flex - reduced height large size 5 (Model/Catalog Number: 783B-5N) is a medical device manufactured by albrecht GmbH. This product is indexed under FDA Product Code / Category Classification Y060309 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 783B-5N
- Product Code / EMDN
- Y060309
- Device Name
- MKS® Osteo
- Database Sync Date
- 2026-08-09 16:28:44
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 MKS Osteo flex - reduced height large size 5?
The registered manufacturer of record for MKS Osteo flex - reduced height large size 5 is albrecht GmbH.
What is the Primary UDI-DI identifier for MKS Osteo flex - reduced height large size 5?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251406607683.
What classification code is assigned to this device?
This device is registered under product classification code Y060309.
Similar Classification Devices (Y060309)
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