eudamed_udi
Primary ID: 08052478983615
SEALSAFE WDLR (UDI 08052478983615)
Manufactured by MILESTONE S.P.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SEALSAFE WDLR - Primary ID 08052478983615
Device Regulatory Overview
The SEALSAFE WDLR (Model/Catalog Number: 68465) is a medical device manufactured by MILESTONE S.P.A.. This product is indexed under FDA Product Code / Category Classification W02079099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 68465
- Product Code / EMDN
- W02079099
- Device Name
- SEALSAFE
- Database Sync Date
- 2026-08-09 18:41:35
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 SEALSAFE WDLR?
The registered manufacturer of record for SEALSAFE WDLR is MILESTONE S.P.A..
What is the Primary UDI-DI identifier for SEALSAFE WDLR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08052478983615.
What classification code is assigned to this device?
This device is registered under product classification code W02079099.
Similar Classification Devices (W02079099)
Other Devices by MILESTONE S.P.A.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint