eudamed_udi
Primary ID: 08050323045020
BiosScrew: instruments tray - Radel supp. (UDI 08050323045020)
Manufactured by Permedica S.p.A
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BiosScrew: instruments tray - Radel supp. - Primary ID 08050323045020
Device Regulatory Overview
The BiosScrew: instruments tray - Radel supp. (Model/Catalog Number: 739201) is a medical device manufactured by Permedica S.p.A. This product is indexed under FDA Product Code / Category Classification S010401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 739201
- Product Code / EMDN
- S010401
- Device Name
- Instruments Tray
- Database Sync Date
- 2026-08-09 16:29:52
Full Regulatory Attributes
π 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 BiosScrew: instruments tray - Radel supp.?
The registered manufacturer of record for BiosScrew: instruments tray - Radel supp. is Permedica S.p.A.
What is the Primary UDI-DI identifier for BiosScrew: instruments tray - Radel supp.?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08050323045020.
What classification code is assigned to this device?
This device is registered under product classification code S010401.
Similar Classification Devices (S010401)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint