GUDIDData
eudamed_udi Primary ID: 07350040974476

CellaVision® DM Software DM1200 Upgrade from 4.0.x to 6.0.x incl. Localization DVD (UDI 07350040974476)

Manufactured by CellaVision AB

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CellaVision® DM Software DM1200 Upgrade from 4.0.x to 6.0.x incl. Localization DVD - Primary ID 07350040974476

Device Regulatory Overview

The CellaVision® DM Software DM1200 Upgrade from 4.0.x to 6.0.x incl. Localization DVD (Model/Catalog Number: CDMS-126040) 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
CDMS-126040
Product Code / EMDN
W02029092
Device Name
CellaVision® DM Software
Database Sync Date
2026-08-09 17:32:08

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® DM Software DM1200 Upgrade from 4.0.x to 6.0.x incl. Localization DVD?

The registered manufacturer of record for CellaVision® DM Software DM1200 Upgrade from 4.0.x to 6.0.x incl. Localization DVD is CellaVision AB.

What is the Primary UDI-DI identifier for CellaVision® DM Software DM1200 Upgrade from 4.0.x to 6.0.x incl. Localization DVD?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07350040974476.

What classification code is assigned to this device?

This device is registered under product classification code W02029092.

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