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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-PENOFINE Pen Needles — 19 UDI-DI variants, MDR

MD Atlas
KD Medical GmbH Hospital Products

Data from EUDAMED, last updated May 23, 2026

KD-PENOFINE Pen Needles

4031881G10-02aIIaUV

19 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: KD Medical GmbH Hospital Products

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 4031881G10-02aIIaUV
Device name: KD-PENOFINE Pen Needles
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
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

19 UDI-DI variants

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Applied filters

basicUdiUlid01KNNXT03ZS99V66Q5DY967Q2P

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

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907009T54031881907004
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907030T54031881907035
904213T54031881904218
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914014T54031881914019
904237T54031881904232
904206T54031881904201