GUDIDData
eudamed_udi Primary ID: 04260767090041

smart pft body (UDI 04260767090041)

Manufactured by medical equipment europe GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for smart pft body - Primary ID 04260767090041

Device Regulatory Overview

The smart pft body (Model/Catalog Number: 13004) is a medical device manufactured by medical equipment europe GmbH. This product is indexed under FDA Product Code / Category Classification Z12159007 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
13004
Product Code / EMDN
Z12159007
Device Name
smart pft body
Database Sync Date
2026-08-09 17:17:05

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 smart pft body?

The registered manufacturer of record for smart pft body is medical equipment europe GmbH.

What is the Primary UDI-DI identifier for smart pft body?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260767090041.

What classification code is assigned to this device?

This device is registered under product classification code Z12159007.

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