GUDIDData
gudid Primary ID: 832-7813-21

8.1MHZ INFANT FL PROBE 841/842 (UDI 832-7813-21)

Manufactured by PARKS MEDICAL ELECTRONICS, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 8.1MHZ INFANT FL PROBE 841/842 - Primary ID 832-7813-21

Device Regulatory Overview

The 8.1MHZ INFANT FL PROBE 841/842 (Model/Catalog Number: 832-7813-21) is a medical device manufactured by PARKS MEDICAL ELECTRONICS, INC.. This product is indexed under FDA Product Code / Category Classification JOP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
832-7813-21
Product Code / EMDN
JOP
Device Name
Database Sync Date
2026-08-09 09:31:28

Full Regulatory Attributes

🔒 Token Gated
{
    "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 8.1MHZ INFANT FL PROBE 841/842?

The registered manufacturer of record for 8.1MHZ INFANT FL PROBE 841/842 is PARKS MEDICAL ELECTRONICS, INC..

What is the Primary UDI-DI identifier for 8.1MHZ INFANT FL PROBE 841/842?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 832-7813-21.

What classification code is assigned to this device?

This device is registered under product classification code JOP.

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