eudamed_udi
Primary ID: 07613365900514
SCHILLER (UDI 07613365900514)
Manufactured by SCHILLER MEDICAL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SCHILLER - Primary ID 07613365900514
Device Regulatory Overview
The SCHILLER (Model/Catalog Number: 1-58-9502) is a medical device manufactured by SCHILLER MEDICAL. This product is indexed under FDA Product Code / Category Classification Z12030503 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1-58-9502
- Product Code / EMDN
- Z12030503
- Device Name
- FRED easy Life Automatic
- Database Sync Date
- 2026-08-09 16:30:38
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 SCHILLER?
The registered manufacturer of record for SCHILLER is SCHILLER MEDICAL.
What is the Primary UDI-DI identifier for SCHILLER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07613365900514.
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 MEDICAL
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint