gudid Primary ID: 017276240863

THE GRINCH (UDI 017276240863)

Manufactured by Aso LLC

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

Scannable UDI-DI Representation

Device Regulatory Overview

The THE GRINCH (Model/Catalog Number: 017276240863) is a medical device manufactured by Aso LLC. This product is indexed under FDA Product Code / Category Classification KGX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 017276240863
Product Code / EMDN: KGX
Device Name: Antibacterial Bandages, assorted shapes & Sizes, 3/4'' strips, 3/4 IN x 3 IN (19 mm x 76 mm), 5/8'' strips, 5/8 IN x 2.1/4 IN (15 mm x57 mm), Ornaments,1.4 IN X 1.22 IN(35 mm x 31 mm)
Database Sync Date: 2026-08-09 09:00:33

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 THE GRINCH?

The registered manufacturer of record for THE GRINCH is Aso LLC.

What is the Primary UDI-DI identifier for THE GRINCH?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 017276240863.

What classification code is assigned to this device?

This device is registered under product classification code KGX.

Similar Classification Devices (KGX)

Other Devices by Aso LLC

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