eudamed_udi
Primary ID: 04260193710223
MOTOmed loop (UDI 04260193710223)
Manufactured by RECK-Technik GmbH & Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MOTOmed loop - Primary ID 04260193710223
Device Regulatory Overview
The MOTOmed loop (Model/Catalog Number: 260.010) is a medical device manufactured by RECK-Technik GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification Z12069099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 260.010
- Product Code / EMDN
- Z12069099
- Device Name
- MOTOmed loop
- Database Sync Date
- 2026-08-09 16:48:01
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 MOTOmed loop?
The registered manufacturer of record for MOTOmed loop is RECK-Technik GmbH & Co. KG.
What is the Primary UDI-DI identifier for MOTOmed loop?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260193710223.
What classification code is assigned to this device?
This device is registered under product classification code Z12069099.
Similar Classification Devices (Z12069099)
Other Devices by RECK-Technik GmbH & Co. KG
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint