gudid Primary ID: RE H 4

CEKA & PRECI-LINE ATTACHMENTS (UDI RE H 4)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The CEKA & PRECI-LINE ATTACHMENTS (Model/Catalog Number: RE H 4) is a medical device manufactured by Alphadent NV. This product is indexed under FDA Product Code / Category Classification EGG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: RE H 4
Product Code / EMDN: EGG
Device Name: REVAX M2 SOLDERING ACC. AXIAL 2 PCS
Database Sync Date: 2026-08-09 09:29:20

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 CEKA & PRECI-LINE ATTACHMENTS?

The registered manufacturer of record for CEKA & PRECI-LINE ATTACHMENTS is Alphadent NV.

What is the Primary UDI-DI identifier for CEKA & PRECI-LINE ATTACHMENTS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RE H 4.

What classification code is assigned to this device?

This device is registered under product classification code EGG.

Similar Classification Devices (EGG)

Other Devices by Alphadent NV

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