eudamed_udi
Primary ID: 04260643584862
EcoFlex (UDI 04260643584862)
Manufactured by Schneider Medical GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EcoFlex - Primary ID 04260643584862
Device Regulatory Overview
The EcoFlex (Model/Catalog Number: N/A) is a medical device manufactured by Schneider Medical GmbH. This product is indexed under FDA Product Code / Category Classification Z12069099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- Z12069099
- Device Name
- Mehrfachkompressen heiß/kalt
- Database Sync Date
- 2026-08-09 16:28:55
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 EcoFlex?
The registered manufacturer of record for EcoFlex is Schneider Medical GmbH.
What is the Primary UDI-DI identifier for EcoFlex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260643584862.
What classification code is assigned to this device?
This device is registered under product classification code Z12069099.
Similar Classification Devices (Z12069099)
Other Devices by Schneider Medical GmbH
Programmatic Export
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JSON API Endpoint