gudid Primary ID: 1

SENTINEL Enteral Feeding Pump (UDI 1)

Manufactured by AMSINO INTERNATIONAL, INC.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The SENTINEL Enteral Feeding Pump (Model/Catalog Number: 1) is a medical device manufactured by AMSINO INTERNATIONAL, INC.. This product is indexed under FDA Product Code / Category Classification LZH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1
Product Code / EMDN: LZH
Device Name
Database Sync Date: 2026-08-09 09:04:15

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 SENTINEL Enteral Feeding Pump?

The registered manufacturer of record for SENTINEL Enteral Feeding Pump is AMSINO INTERNATIONAL, INC..

What is the Primary UDI-DI identifier for SENTINEL Enteral Feeding Pump?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.

What classification code is assigned to this device?

This device is registered under product classification code LZH.

Similar Classification Devices (LZH)

Other Devices by AMSINO INTERNATIONAL, INC.

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