GUDIDData
Bulk Audit Tool API Access
gudid Primary ID: 306030-0000-000

SMARTDRAPE (UDI 306030-0000-000)

Manufactured by Carl Zeiss Meditec AG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SMARTDRAPE - Primary ID 306030-0000-000

Device Regulatory Overview

The SMARTDRAPE (Model/Catalog Number: 306030-0000-000) is a medical device manufactured by Carl Zeiss Meditec AG. This product is indexed under FDA Product Code / Category Classification PUI 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
306030-0000-000
Product Code / EMDN
PUI
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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Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

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Frequently Asked Questions

Who is the primary manufacturer of SMARTDRAPE?

The registered manufacturer of record for SMARTDRAPE is Carl Zeiss Meditec AG.

What is the Primary UDI-DI identifier for SMARTDRAPE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 306030-0000-000.

What classification code is assigned to this device?

This device is registered under product classification code PUI.

Similar Classification Devices (PUI)

Other Devices by Carl Zeiss Meditec AG

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint