eudamed_udi Primary ID: 09330453301203

INSUFFLATOR FILTER TUBING (UDI 09330453301203)

Manufactured by Fairmont Medical Products Pty Ltd

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

Scannable UDI-DI Representation

Device Regulatory Overview

The INSUFFLATOR FILTER TUBING (Model/Catalog Number: DIF7002) is a medical device manufactured by Fairmont Medical Products Pty Ltd. This product is indexed under FDA Product Code / Category Classification R040101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DIF7002
Product Code / EMDN: R040101
Device Name: INSUFFLATOR FILTER TUBING
Database Sync Date: 2026-08-09 16:29:21

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 INSUFFLATOR FILTER TUBING?

The registered manufacturer of record for INSUFFLATOR FILTER TUBING is Fairmont Medical Products Pty Ltd.

What is the Primary UDI-DI identifier for INSUFFLATOR FILTER TUBING?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09330453301203.

What classification code is assigned to this device?

This device is registered under product classification code R040101.

Similar Classification Devices (R040101)

Other Devices by Fairmont Medical Products Pty Ltd

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