eudamed_udi
Primary ID: 04251406606921
MKS Osteo plus medium size 1 (UDI 04251406606921)
Manufactured by albrecht GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MKS Osteo plus medium size 1 - Primary ID 04251406606921
Device Regulatory Overview
The MKS Osteo plus medium size 1 (Model/Catalog Number: 784A-1) 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
- 784A-1
- Product Code / EMDN
- Y060309
- Device Name
- MKS® Osteo
- Database Sync Date
- 2026-08-09 16:28:54
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 plus medium size 1?
The registered manufacturer of record for MKS Osteo plus medium size 1 is albrecht GmbH.
What is the Primary UDI-DI identifier for MKS Osteo plus medium size 1?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251406606921.
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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