eudamed_udi Primary ID: 07612367017138

Unspecified Brand (UDI 07612367017138)

Manufactured by Medela AG

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: 077.0140) is a medical device manufactured by Medela AG. This product is indexed under FDA Product Code / Category Classification Z12080399 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 077.0140
Product Code / EMDN: Z12080399
Device Name: Manual Vacuum Extractor Sets
Database Sync Date: 2026-08-09 17:14:43

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is Medela AG.

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07612367017138.

What classification code is assigned to this device?

This device is registered under product classification code Z12080399.

Similar Classification Devices (Z12080399)

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