GUDIDData
gudid Primary ID: ULTRASOUND LOTION

POLYSONIC (UDI ULTRASOUND LOTION)

Manufactured by PARKER LABORATORIES INC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for POLYSONIC - Primary ID ULTRASOUND LOTION

Device Regulatory Overview

The POLYSONIC (Model/Catalog Number: ULTRASOUND LOTION) is a medical device manufactured by PARKER LABORATORIES INC. This product is indexed under FDA Product Code / Category Classification IYO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ULTRASOUND LOTION
Product Code / EMDN
IYO
Device Name
Polysonic Ultrasound Lotion, 250 ml bottle
Database Sync Date
2026-08-09 09:49:29

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 POLYSONIC?

The registered manufacturer of record for POLYSONIC is PARKER LABORATORIES INC.

What is the Primary UDI-DI identifier for POLYSONIC?

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

What classification code is assigned to this device?

This device is registered under product classification code IYO.

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