gudid Primary ID: 8.1

CAAS Workstation (UDI 8.1)

Manufactured by Pie Medical Imaging B.V.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The CAAS Workstation (Model/Catalog Number: 8.1) is a medical device manufactured by Pie Medical Imaging B.V.. This product is indexed under FDA Product Code / Category Classification LLZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 8.1
Product Code / EMDN: LLZ
Device Name
Database Sync Date: 2026-08-09 09:04:29

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 CAAS Workstation?

The registered manufacturer of record for CAAS Workstation is Pie Medical Imaging B.V..

What is the Primary UDI-DI identifier for CAAS Workstation?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8.1.

What classification code is assigned to this device?

This device is registered under product classification code LLZ.

Similar Classification Devices (LLZ)

Other Devices by Pie Medical Imaging B.V.

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