GUDIDData
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eudamed_udi Primary ID: 08681277822117

Mediflex (UDI 08681277822117)

Manufactured by Mediflex Medikal

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Mediflex - Primary ID 08681277822117

Device Regulatory Overview

The Mediflex (Model/Catalog Number: FP 623-010) is a medical device manufactured by Mediflex Medikal. This product is indexed under FDA Product Code / Category Classification R02010101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
FP 623-010
Product Code / EMDN
R02010101
Device Name
Anesthesia Breathing Circuits
Database Sync Date
2026-08-09 17:12:06

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 Mediflex?

The registered manufacturer of record for Mediflex is Mediflex Medikal.

What is the Primary UDI-DI identifier for Mediflex?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681277822117.

What classification code is assigned to this device?

This device is registered under product classification code R02010101.

Similar Classification Devices (R02010101)

Other Devices by Mediflex Medikal

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