gudid Primary ID: 40712050

DrillCut-X (UDI 40712050)

Manufactured by Karl Storz GmbH & Co. KG

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

Scannable UDI-DI Representation

Device Regulatory Overview

The DrillCut-X (Model/Catalog Number: 40712050) is a medical device manufactured by Karl Storz GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification ERL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 40712050
Product Code / EMDN: ERL
Device Name: DrillCut-X II Shaver Handpiece
Database Sync Date: 2026-08-09 09:11:33

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 DrillCut-X?

The registered manufacturer of record for DrillCut-X is Karl Storz GmbH & Co. KG.

What is the Primary UDI-DI identifier for DrillCut-X?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 40712050.

What classification code is assigned to this device?

This device is registered under product classification code ERL.

Similar Classification Devices (ERL)

Other Devices by Karl Storz GmbH & Co. KG

Programmatic Export

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

JSON API Endpoint