GUDIDData
eudamed_udi Primary ID: +D7701126853

Sweden & Martina (UDI +D7701126853)

Manufactured by SWEDEN & MARTINA S.P.A.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sweden & Martina - Primary ID +D7701126853

Device Regulatory Overview

The Sweden & Martina (Model/Catalog Number: E-MPSCI-500) is a medical device manufactured by SWEDEN & MARTINA S.P.A.. This product is indexed under FDA Product Code / Category Classification P010299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
E-MPSCI-500
Product Code / EMDN
P010299
Device Name
Prosthetic Component
Database Sync Date
2026-08-09 16:29:12

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 Sweden & Martina?

The registered manufacturer of record for Sweden & Martina is SWEDEN & MARTINA S.P.A..

What is the Primary UDI-DI identifier for Sweden & Martina?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +D7701126853.

What classification code is assigned to this device?

This device is registered under product classification code P010299.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint