eudamed_udi Primary ID: 08015262008482

Siringa enterale 20 ml- NUTRIFIT (riutilizzabile) (UDI 08015262008482)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Siringa enterale 20 ml- NUTRIFIT (riutilizzabile) (Model/Catalog Number: 1012.207) is a medical device manufactured by PENTAFERTE ITALIA SRL. This product is indexed under FDA Product Code / Category Classification A020108 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1012.207
Product Code / EMDN: A020108
Device Name: SIRINGHE E ACCESSORI ENTERALI
Database Sync Date: 2026-08-09 17:03:05

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 Siringa enterale 20 ml- NUTRIFIT (riutilizzabile)?

The registered manufacturer of record for Siringa enterale 20 ml- NUTRIFIT (riutilizzabile) is PENTAFERTE ITALIA SRL.

What is the Primary UDI-DI identifier for Siringa enterale 20 ml- NUTRIFIT (riutilizzabile)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08015262008482.

What classification code is assigned to this device?

This device is registered under product classification code A020108.

Similar Classification Devices (A020108)

Other Devices by PENTAFERTE ITALIA SRL

Programmatic Export

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

JSON API Endpoint