eudamed_udi
Primary ID: 07613365001921
FRED Easyport plus (UDI 07613365001921)
Manufactured by SCHILLER AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FRED Easyport plus - Primary ID 07613365001921
Device Regulatory Overview
The FRED Easyport plus (Model/Catalog Number: 3.940060) is a medical device manufactured by SCHILLER AG. This product is indexed under FDA Product Code / Category Classification Z12030503 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3.940060
- Product Code / EMDN
- Z12030503
- Device Name
- FRED Easyport plus
- Database Sync Date
- 2026-08-09 18:35:10
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 FRED Easyport plus?
The registered manufacturer of record for FRED Easyport plus is SCHILLER AG.
What is the Primary UDI-DI identifier for FRED Easyport plus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07613365001921.
What classification code is assigned to this device?
This device is registered under product classification code Z12030503.
Similar Classification Devices (Z12030503)
Other Devices by SCHILLER AG
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