eudamed_udi
Primary ID: 05901247378028
AKZ-1 (SS) (UDI 05901247378028)
Manufactured by SteelBo Sp.z o.o.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AKZ-1 (SS) - Primary ID 05901247378028
Device Regulatory Overview
The AKZ-1 (SS) (Model/Catalog Number: AKZ-1 (SS)) is a medical device manufactured by SteelBo Sp.z o.o.. This product is indexed under FDA Product Code / Category Classification Y062499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AKZ-1 (SS)
- Product Code / EMDN
- Y062499
- Device Name
- Adaptery łączące (zaciskowe)
- Database Sync Date
- 2026-08-09 16:28:53
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 AKZ-1 (SS)?
The registered manufacturer of record for AKZ-1 (SS) is SteelBo Sp.z o.o..
What is the Primary UDI-DI identifier for AKZ-1 (SS)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05901247378028.
What classification code is assigned to this device?
This device is registered under product classification code Y062499.
Similar Classification Devices (Y062499)
Other Devices by SteelBo Sp.z o.o.
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