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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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Hydrozid FORCE — 2 UDI-DI variants, MDR (BIBAWO Medical A/S)

MD Atlas
BIBAWO Medical A/S

Data from EUDAMED, last updated May 31, 2026

Hydrozid FORCE

574400242Hydrozid2013NE

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: BIBAWO Medical A/S

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 574400242Hydrozid2013NE
Device name: Hydrozid FORCE
Device model: FORCE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Sep 26, 2022

Manufacturer & authorised representative

Manufacturer

Name: BIBAWO Medical A/S
SRN: DK-MF-000024659
Country: Denmark
Email: quality@bibawo-medical.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GA3JBRRYDDYV9VPT1HG7WAAN

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

Hydrozid FORCE05744002420002
20105744002424024