gudid Primary ID: SHRP-3003-001

PancreasPak (UDI SHRP-3003-001)

Manufactured by Paragonix Technologies Inc

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PancreasPak (Model/Catalog Number: SHRP-3003-001) is a medical device manufactured by Paragonix Technologies Inc. This product is indexed under FDA Product Code / Category Classification KDN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: SHRP-3003-001
Product Code / EMDN: KDN
Device Name: PancreasPak Shipper Base
Database Sync Date: 2026-08-09 09:37:49

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 PancreasPak?

The registered manufacturer of record for PancreasPak is Paragonix Technologies Inc.

What is the Primary UDI-DI identifier for PancreasPak?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SHRP-3003-001.

What classification code is assigned to this device?

This device is registered under product classification code KDN.

Similar Classification Devices (KDN)

Other Devices by Paragonix Technologies Inc

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