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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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Velara Family — 3 UDI-DI variants, MDR

MD Atlas
Philips Medical Systems DMC GmbH

Data from EUDAMED, last updated May 23, 2026

Velara Family

0884838BM499TT

3 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: Philips Medical Systems DMC GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 0884838BM499TT
Device name: Velara Family
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jul 25, 2025

Manufacturer & authorised representative

Manufacturer

Name: Philips Medical Systems DMC GmbH
SRN: DE-MF-000005362
Country: Germany
Email: eudamed@philips.com
Phone: n/a

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K10JSYRDS6367WRZ1QVG8SQT

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

Velara CVFD00884838076129
Velara GCF 2T00884838076150
Velara R/F 2T00884838076143