eudamed_udi
Primary ID: 04262466450096
ALDS PRO (UDI 04262466450096)
Manufactured by Lothar Medtec GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ALDS PRO - Primary ID 04262466450096
Device Regulatory Overview
The ALDS PRO (Model/Catalog Number: ALDS PRO) 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 PRO
- Product Code / EMDN
- Z12159080
- Device Name
- ALDS
- Database Sync Date
- 2026-08-09 17:18:01
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ALDS PRO?
The registered manufacturer of record for ALDS PRO is Lothar Medtec GmbH.
What is the Primary UDI-DI identifier for ALDS PRO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04262466450096.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint