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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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KD-FINE BLUNT — 9 UDI-DI variants, MDR

MD Atlas
KD Medical GmbH Hospital Products

Data from EUDAMED, last updated May 23, 2026

KD-FINE BLUNT

4031881G11-01IsMJ

9 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: KD Medical GmbH Hospital Products

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 4031881G11-01IsMJ
Device name: KD-FINE BLUNT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: KD Medical GmbH Hospital Products
SRN: DE-MF-000006773
Country: Germany
Email: info@kdm-berlin.de

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01KNP14QJB05PV8HM2J02SKR6D

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

91714524031881917149
90797924031881907973
90796224031881907966
91059724031881910591
90929424031881909298
909300A54031881909305
92028224031881920286
910603A54031881910608
92029924031881920293