eudamed_udi Primary ID: 05940652026650

SUPLIMENT PENTRU CLOSTRIDIUM DIFICILE (UDI 05940652026650)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The SUPLIMENT PENTRU CLOSTRIDIUM DIFICILE (Model/Catalog Number: S014.81007) is a medical device manufactured by SC MEDICAMED MARKET SRL. This product is indexed under FDA Product Code / Category Classification W0104010104 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: S014.81007
Product Code / EMDN: W0104010104
Device Name: SUPLIMENT PENTRU CLOSTRIDIUM DIFICILE
Database Sync Date: 2026-08-09 17:04:34

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 SUPLIMENT PENTRU CLOSTRIDIUM DIFICILE?

The registered manufacturer of record for SUPLIMENT PENTRU CLOSTRIDIUM DIFICILE is SC MEDICAMED MARKET SRL.

What is the Primary UDI-DI identifier for SUPLIMENT PENTRU CLOSTRIDIUM DIFICILE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05940652026650.

What classification code is assigned to this device?

This device is registered under product classification code W0104010104.

Similar Classification Devices (W0104010104)

Other Devices by SC MEDICAMED MARKET SRL

Programmatic Export

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

JSON API Endpoint