GUDIDData
eudamed_udi Primary ID: +EBAN7933100-

TRISON TE 4000 DU (UDI +EBAN7933100-)

Manufactured by BANDELIN electronic GmbH & Co. KG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TRISON TE 4000 DU - Primary ID +EBAN7933100-

Device Regulatory Overview

The TRISON TE 4000 DU (Model/Catalog Number: 793310) is a medical device manufactured by BANDELIN electronic GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification Z12011302 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
793310
Product Code / EMDN
Z12011302
Device Name
TRISON High-performance ultrasonic bath
Database Sync Date
2026-08-09 16:45:05

Full Regulatory Attributes

đź”’ Token Gated
{
    "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 TRISON TE 4000 DU?

The registered manufacturer of record for TRISON TE 4000 DU is BANDELIN electronic GmbH & Co. KG.

What is the Primary UDI-DI identifier for TRISON TE 4000 DU?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +EBAN7933100-.

What classification code is assigned to this device?

This device is registered under product classification code Z12011302.

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