GUDIDData
eudamed_udi Primary ID: 07350040974575

CellaVision® Remote Review Group Edition License upgrade from Team to Group Edition (UDI 07350040974575)

Manufactured by CellaVision AB

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CellaVision® Remote Review Group Edition License upgrade from Team to Group Edition - Primary ID 07350040974575

Device Regulatory Overview

The CellaVision® Remote Review Group Edition License upgrade from Team to Group Edition (Model/Catalog Number: CRRS-GRTE99) is a medical device manufactured by CellaVision AB. This product is indexed under FDA Product Code / Category Classification W02029092 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CRRS-GRTE99
Product Code / EMDN
W02029092
Device Name
CellaVision® Review Software
Database Sync Date
2026-08-09 17:52:28

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 CellaVision® Remote Review Group Edition License upgrade from Team to Group Edition?

The registered manufacturer of record for CellaVision® Remote Review Group Edition License upgrade from Team to Group Edition is CellaVision AB.

What is the Primary UDI-DI identifier for CellaVision® Remote Review Group Edition License upgrade from Team to Group Edition?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07350040974575.

What classification code is assigned to this device?

This device is registered under product classification code W02029092.

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