eudamed_udi Primary ID: 08053904509201

CALZE ELASTICHE TERAPEUTICHE K2 (UDI 08053904509201)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The CALZE ELASTICHE TERAPEUTICHE K2 (Model/Catalog Number: 412ABG5) is a medical device manufactured by SAFTE S.r.l.. This product is indexed under FDA Product Code / Category Classification M030405 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 412ABG5
Product Code / EMDN: M030405
Device Name: CALZE
Database Sync Date: 2026-08-09 16:28:48

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 CALZE ELASTICHE TERAPEUTICHE K2?

The registered manufacturer of record for CALZE ELASTICHE TERAPEUTICHE K2 is SAFTE S.r.l..

What is the Primary UDI-DI identifier for CALZE ELASTICHE TERAPEUTICHE K2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053904509201.

What classification code is assigned to this device?

This device is registered under product classification code M030405.

Similar Classification Devices (M030405)

Other Devices by SAFTE S.r.l.

Programmatic Export

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

JSON API Endpoint