eudamed_udi
Primary ID: 04262466450034
ALDS Software (UDI 04262466450034)
Manufactured by Lothar Medtec GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ALDS Software - Primary ID 04262466450034
Device Regulatory Overview
The ALDS Software (Model/Catalog Number: ALDS Software) is a medical device manufactured by Lothar Medtec GmbH. This product is indexed under FDA Product Code / Category Classification Z12159092 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ALDS Software
- Product Code / EMDN
- Z12159092
- Device Name
- ALDS
- Database Sync Date
- 2026-08-09 18:08:32
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 ALDS Software?
The registered manufacturer of record for ALDS Software is Lothar Medtec GmbH.
What is the Primary UDI-DI identifier for ALDS Software?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04262466450034.
What classification code is assigned to this device?
This device is registered under product classification code Z12159092.
Similar Classification Devices (Z12159092)
Other Devices by Lothar Medtec GmbH
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