gudid Primary ID: E-1203SP

Alcor SENTINELplus (UDI E-1203SP)

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-1203SP) 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-1203SP
Product Code / EMDN: KNT
Device Name: Enteral feeding gravity set, NS
Database Sync Date: 2026-08-09 09:46:58

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 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-1203SP.

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.

Programmatic Export

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

JSON API Endpoint