GUDIDData
eudamed_udi Primary ID: 04057155000337

Rotationsflowgeber (UDI 04057155000337)

Manufactured by eResearchTechnology GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rotationsflowgeber - Primary ID 04057155000337

Device Regulatory Overview

The Rotationsflowgeber (Model/Catalog Number: 1413xx) is a medical device manufactured by eResearchTechnology GmbH. This product is indexed under FDA Product Code / Category Classification Z12150102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1413xx
Product Code / EMDN
Z12150102
Device Name
Asthma Monitor
Database Sync Date
2026-08-09 16:51:02

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 Rotationsflowgeber?

The registered manufacturer of record for Rotationsflowgeber is eResearchTechnology GmbH.

What is the Primary UDI-DI identifier for Rotationsflowgeber?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04057155000337.

What classification code is assigned to this device?

This device is registered under product classification code Z12150102.

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