GUDIDData
gudid Primary ID: 22-0117-0202-25

PharmGuard (UDI 22-0117-0202-25)

Manufactured by ICU MEDICAL, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PharmGuard - Primary ID 22-0117-0202-25

Device Regulatory Overview

The PharmGuard (Model/Catalog Number: 22-0117-0202-25) is a medical device manufactured by ICU MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification MRZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
22-0117-0202-25
Product Code / EMDN
MRZ
Device Name
Database Sync Date
2026-08-09 09:29:11

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 PharmGuard?

The registered manufacturer of record for PharmGuard is ICU MEDICAL, INC..

What is the Primary UDI-DI identifier for PharmGuard?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 22-0117-0202-25.

What classification code is assigned to this device?

This device is registered under product classification code MRZ.

Programmatic Export

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

JSON API Endpoint