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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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Unihaft® — 4 UDI-DI variants, MDR (BSN medical GmbH)

MD Atlas
BSN medical GmbH

Data from EUDAMED, last updated May 23, 2026

Unihaft®

404280940039686AQ

4 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: BSN medical GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 404280940039686AQ
Device name: Unihaft®
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: BSN medical GmbH
SRN: DE-MF-000005787
Country: Germany
Email: EUDAMEDinfo_medical@essity.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KRX7H92QGDC6W0T2M4GPS5P7

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

45899-0004042809077100
45897-0004042809077049
45896-0004042809077018
45898-0004042809077070