GUDIDData
eudamed_udi Primary ID: 07640229295622

Subtilis Beckenhebel mit Propylux® Kunststoffgriff 26 x 120 mm, 38 cm, Nr. 57 mit Gewichtsschlitz (UDI 07640229295622)

Manufactured by Accuratus AG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Subtilis Beckenhebel mit Propylux® Kunststoffgriff 26 x 120 mm, 38 cm, Nr. 57 mit Gewichtsschlitz - Primary ID 07640229295622

Device Regulatory Overview

The Subtilis Beckenhebel mit Propylux® Kunststoffgriff 26 x 120 mm, 38 cm, Nr. 57 mit Gewichtsschlitz (Model/Catalog Number: 24.51.91) is a medical device manufactured by Accuratus AG. This product is indexed under FDA Product Code / Category Classification L0902 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
24.51.91
Product Code / EMDN
L0902
Device Name
Subtilis Beckenhebel mit Propylux® Kunststoffgriff 26 x 120 mm, 38 cm, Nr. 57 mit Gewichtsschlitz
Database Sync Date
2026-08-09 16:30:01

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 Subtilis Beckenhebel mit Propylux® Kunststoffgriff 26 x 120 mm, 38 cm, Nr. 57 mit Gewichtsschlitz?

The registered manufacturer of record for Subtilis Beckenhebel mit Propylux® Kunststoffgriff 26 x 120 mm, 38 cm, Nr. 57 mit Gewichtsschlitz is Accuratus AG.

What is the Primary UDI-DI identifier for Subtilis Beckenhebel mit Propylux® Kunststoffgriff 26 x 120 mm, 38 cm, Nr. 57 mit Gewichtsschlitz?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07640229295622.

What classification code is assigned to this device?

This device is registered under product classification code L0902.

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