GUDIDData
eudamed_udi Primary ID: 04260754971704

FastExtract® MX AS1-Extraktor L. 150 mm Für abgebrochene Schrauben ID. 3.6 mm / Für Gewinde Ø 2.0 - 3.5 mm (UDI 04260754971704)

Manufactured by Ortho-Medicor Aktiengesellschaft

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FastExtract® MX AS1-Extraktor L. 150 mm Für abgebrochene Schrauben ID. 3.6 mm / Für Gewinde Ø 2.0 - 3.5 mm - Primary ID 04260754971704

Device Regulatory Overview

The FastExtract® MX AS1-Extraktor L. 150 mm Für abgebrochene Schrauben ID. 3.6 mm / Für Gewinde Ø 2.0 - 3.5 mm (Model/Catalog Number: 150-7132-001) is a medical device manufactured by Ortho-Medicor Aktiengesellschaft. This product is indexed under FDA Product Code / Category Classification L091101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
150-7132-001
Product Code / EMDN
L091101
Device Name
Extraktor
Database Sync Date
2026-08-09 16:44:55

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 FastExtract® MX AS1-Extraktor L. 150 mm Für abgebrochene Schrauben ID. 3.6 mm / Für Gewinde Ø 2.0 - 3.5 mm?

The registered manufacturer of record for FastExtract® MX AS1-Extraktor L. 150 mm Für abgebrochene Schrauben ID. 3.6 mm / Für Gewinde Ø 2.0 - 3.5 mm is Ortho-Medicor Aktiengesellschaft.

What is the Primary UDI-DI identifier for FastExtract® MX AS1-Extraktor L. 150 mm Für abgebrochene Schrauben ID. 3.6 mm / Für Gewinde Ø 2.0 - 3.5 mm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260754971704.

What classification code is assigned to this device?

This device is registered under product classification code L091101.

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