eudamed_udi
Primary ID: 08710685112456
TOTAAL HEUP TRAY (UDI 08710685112456)
Manufactured by Medica Europe B.V.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TOTAAL HEUP TRAY - Primary ID 08710685112456
Device Regulatory Overview
The TOTAAL HEUP TRAY (Model/Catalog Number: 115250AK) is a medical device manufactured by Medica Europe B.V.. This product is indexed under FDA Product Code / Category Classification V0599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 115250AK
- Product Code / EMDN
- V0599
- Device Name
- Custom Procedure Trays
- Database Sync Date
- 2026-08-09 16:28:45
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 TOTAAL HEUP TRAY?
The registered manufacturer of record for TOTAAL HEUP TRAY is Medica Europe B.V..
What is the Primary UDI-DI identifier for TOTAAL HEUP TRAY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08710685112456.
What classification code is assigned to this device?
This device is registered under product classification code V0599.
Similar Classification Devices (V0599)
Other Devices by Medica Europe B.V.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint