gudid Primary ID: 26001 150ml

AxioSil Putty (UDI 26001 150ml)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The AxioSil Putty (Model/Catalog Number: 26001 150ml) is a medical device manufactured by Axiodent Inc.. This product is indexed under FDA Product Code / Category Classification ELW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 26001 150ml
Product Code / EMDN: ELW
Device Name
Database Sync Date: 2026-08-09 09:01:55

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 AxioSil Putty?

The registered manufacturer of record for AxioSil Putty is Axiodent Inc..

What is the Primary UDI-DI identifier for AxioSil Putty?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 26001 150ml.

What classification code is assigned to this device?

This device is registered under product classification code ELW.

Similar Classification Devices (ELW)

Other Devices by Axiodent Inc.

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