eudamed_udi
Primary ID: 05901780411398
Unspecified Brand (UDI 05901780411398)
Manufactured by mdh sp. z o. o.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 05901780411398
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: DRIE0ALAXXULP) is a medical device manufactured by mdh sp. z o. o.. This product is indexed under FDA Product Code / Category Classification Y061299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DRIE0ALAXXULP
- Product Code / EMDN
- Y061299
- Device Name
- Hallustop
- Database Sync Date
- 2026-08-09 16:28:51
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 mdh sp. z o. o..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05901780411398.
What classification code is assigned to this device?
This device is registered under product classification code Y061299.
Similar Classification Devices (Y061299)
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