gudid Primary ID: 1015.1007

NUTRIFIT (UDI 1015.1007)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The NUTRIFIT (Model/Catalog Number: 1015.1007) is a medical device manufactured by PENTAFERTE ITALIA SRL. This product is indexed under FDA Product Code / Category Classification PNR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1015.1007
Product Code / EMDN: PNR
Device Name: Enteral ENFit syringe 100ml
Database Sync Date: 2026-08-09 09:05:06

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of NUTRIFIT?

The registered manufacturer of record for NUTRIFIT is PENTAFERTE ITALIA SRL.

What is the Primary UDI-DI identifier for NUTRIFIT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1015.1007.

What classification code is assigned to this device?

This device is registered under product classification code PNR.

Similar Classification Devices (PNR)

Other Devices by PENTAFERTE ITALIA SRL

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