gudid Primary ID: 26-310

GET SCULPTED (UDI 26-310)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The GET SCULPTED (Model/Catalog Number: 26-310) is a medical device manufactured by PASCAL COMPANY, INC.. This product is indexed under FDA Product Code / Category Classification EIK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 26-310
Product Code / EMDN: EIK
Device Name: Wax Carving Set
Database Sync Date: 2026-08-09 09:20:12

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 GET SCULPTED?

The registered manufacturer of record for GET SCULPTED is PASCAL COMPANY, INC..

What is the Primary UDI-DI identifier for GET SCULPTED?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 26-310.

What classification code is assigned to this device?

This device is registered under product classification code EIK.

Similar Classification Devices (EIK)

Other Devices by PASCAL COMPANY, INC.

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