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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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BD Cato Prescribe — 4 UDI-DI variants, MDR

MD Atlas
Becton Dickinson Austria GmbH

Data from EUDAMED, last updated May 23, 2026

BD Cato Prescribe

0885403CVBTYVWAD5

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Becton Dickinson Austria GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 0885403CVBTYVWAD5
Device name: BD Cato Prescribe
Device model: BD Cato Prescribe
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Jul 14, 2025

Manufacturer & authorised representative

Manufacturer

Name: Becton Dickinson Austria GmbH
SRN: AT-MF-000002652
Country: Austria
Email: cato_office@bd.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K04KGHAP535B5H12P7PZ9MG0

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

MED_WF_SFW_SOL250 10885403502620
BD Cato Prescribe10885403521447
MED_WF_SFW_SOL25210885403510229
BD Cato Prescribe10885403493430