gudid Primary ID: E-1004SP

Alcor SENTINELplus (UDI E-1004SP)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Alcor SENTINELplus (Model/Catalog Number: E-1004SP) is a medical device manufactured by ALCOR SCIENTIFIC INC.. This product is indexed under FDA Product Code / Category Classification KNT within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: E-1004SP
Product Code / EMDN: KNT
Device Name: Enteral Feeding Pump Spike Set, NS
Database Sync Date: 2026-08-09 09:46:58

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 Alcor SENTINELplus?

The registered manufacturer of record for Alcor SENTINELplus is ALCOR SCIENTIFIC INC..

What is the Primary UDI-DI identifier for Alcor SENTINELplus?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is E-1004SP.

What classification code is assigned to this device?

This device is registered under product classification code KNT.

Similar Classification Devices (KNT)

Other Devices by ALCOR SCIENTIFIC INC.

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