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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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CellaVision® DC-1 — 1 UDI-DI variant, IVDR (CellaVision AB)

MD Atlas
CellaVision AB

Data from EUDAMED, last updated May 31, 2026

CellaVision® DC-1

735004097XU-10301AH

1 UDI-DI variant

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: CellaVision AB

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 735004097XU-10301AH
Device name: CellaVision® DC-1
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: CellaVision AB
SRN: SE-MF-000002377
Country: Sweden
Email: johan.attelid@cellavision.se
Phone: +46761611390

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KPWY7M161AV8MTM808HN6AE5

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

CellaVision® DC-107350040975091