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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 S Pen Needles — 11 UDI-DI variants, MDR

MD Atlas
KD Medical GmbH Hospital Products

Data from EUDAMED, last updated May 23, 2026

KD-PENOFINE S Pen Needles

4031881G10-02bIIaV4

11 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: 4031881G10-02bIIaV4
Device name: KD-PENOFINE S 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

11 UDI-DI variants

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Applied filters

basicUdiUlid01KNNZ1XE1T9DAJC9WT1TSFBAN

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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92002224031881920026
92004624031881920040
92022024031881920224
92001524031881920019
91997224031881919976
91996524031881919969
91999624031881919990
92018324031881920187
92019024031881920194
92003924031881920033