eudamed_udi
Primary ID: 04262466450041
ALDS (UDI 04262466450041)
Manufactured by Lothar Medtec GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ALDS - Primary ID 04262466450041
Device Regulatory Overview
The ALDS (Model/Catalog Number: ALDS) is a medical device manufactured by Lothar Medtec GmbH. This product is indexed under FDA Product Code / Category Classification Z12159080 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ALDS
- Product Code / EMDN
- Z12159080
- Device Name
- ALDS
- Database Sync Date
- 2026-08-09 18:19:34
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?
The registered manufacturer of record for ALDS is Lothar Medtec GmbH.
What is the Primary UDI-DI identifier for ALDS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04262466450041.
What classification code is assigned to this device?
This device is registered under product classification code Z12159080.
Similar Classification Devices (Z12159080)
Other Devices by Lothar Medtec GmbH
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