eudamed_udi
Primary ID: +G053OMAMDR0B
Oldenburger Mesprogramme (UDI +G053OMAMDR0B)
Manufactured by Hörzentrum Oldenburg gGmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Oldenburger Mesprogramme - Primary ID +G053OMAMDR0B
Device Regulatory Overview
The Oldenburger Mesprogramme (Model/Catalog Number: OMA 2.0.2) is a medical device manufactured by Hörzentrum Oldenburg gGmbH. This product is indexed under FDA Product Code / Category Classification Z121401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- OMA 2.0.2
- Product Code / EMDN
- Z121401
- Device Name
- Oldenburger Messprogramme
- Database Sync Date
- 2026-08-09 16:51:33
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 Oldenburger Mesprogramme?
The registered manufacturer of record for Oldenburger Mesprogramme is Hörzentrum Oldenburg gGmbH.
What is the Primary UDI-DI identifier for Oldenburger Mesprogramme?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +G053OMAMDR0B.
What classification code is assigned to this device?
This device is registered under product classification code Z121401.
Similar Classification Devices (Z121401)
Other Devices by Hörzentrum Oldenburg gGmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint