eudamed_udi Primary ID: 03322541049643

MANUGIB 3D D T4D (UDI 03322541049643)

Manufactured by GIBAUD

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

Scannable UDI-DI Representation

Device Regulatory Overview

The MANUGIB 3D D T4D (Model/Catalog Number: 6700-4D) is a medical device manufactured by GIBAUD. This product is indexed under FDA Product Code / Category Classification Y060612 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 6700-4D
Product Code / EMDN: Y060612
Device Name: MANUGIB 3D D T1D
Database Sync Date: 2026-08-09 16:28:51

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 MANUGIB 3D D T4D?

The registered manufacturer of record for MANUGIB 3D D T4D is GIBAUD.

What is the Primary UDI-DI identifier for MANUGIB 3D D T4D?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03322541049643.

What classification code is assigned to this device?

This device is registered under product classification code Y060612.

Similar Classification Devices (Y060612)

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