eudamed_udi
Primary ID: 05902643958500
Unspecified Brand (UDI 05902643958500)
Manufactured by BioMaxima Spółka Akcyjna
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 05902643958500
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 1-337-K010) is a medical device manufactured by BioMaxima Spółka Akcyjna. This product is indexed under FDA Product Code / Category Classification W0102160511 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1-337-K010
- Product Code / EMDN
- W0102160511
- Device Name
- Test panelowy 10 10 testów AMP/COC/OPI/THC/MET/BAR/BZO/TCA/MTD/PCP
- Database Sync Date
- 2026-08-09 16:28:50
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is BioMaxima Spółka Akcyjna.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05902643958500.
What classification code is assigned to this device?
This device is registered under product classification code W0102160511.
Similar Classification Devices (W0102160511)
Other Devices by BioMaxima Spółka Akcyjna
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