GUDIDData
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gudid Primary ID: 304534-6000-562

INTRABEAM Spherical Applicator 4.0 cm (UDI 304534-6000-562)

Manufactured by Carl Zeiss Meditec AG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for INTRABEAM Spherical Applicator 4.0 cm - Primary ID 304534-6000-562

Device Regulatory Overview

The INTRABEAM Spherical Applicator 4.0 cm (Model/Catalog Number: 304534-6000-562) is a medical device manufactured by Carl Zeiss Meditec AG. This product is indexed under FDA Product Code / Category Classification JAD within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2649-2026 View Full Alert →

Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-1153-2014 View Full Alert →

Treatment packs used on the VisuMax Laser Keratome. Size M Manufactured by Carl Zeiss Meditec AG, Jena, Germany. The VisuMax Laser K...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-1049-2015 View Full Alert →

FORUM Archive and Viewer, version 3.1, v 3.1.1, (DVD Format) and v 3.2, v 3.2.1.(DVD and USB Flash Drive Format). Catalog numbers: 00000...

🔒 Compromised Lot & Serial Numbers Locked
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Technical Specifications

Model Number
304534-6000-562
Product Code / EMDN
JAD
Device Name
Database Sync Date
2026-08-09 09:11:22

Full Regulatory Attributes

🔒 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 INTRABEAM Spherical Applicator 4.0 cm?

The registered manufacturer of record for INTRABEAM Spherical Applicator 4.0 cm is Carl Zeiss Meditec AG.

What is the Primary UDI-DI identifier for INTRABEAM Spherical Applicator 4.0 cm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 304534-6000-562.

What classification code is assigned to this device?

This device is registered under product classification code JAD.

Similar Classification Devices (JAD)

Other Devices by Carl Zeiss Meditec AG

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