Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

KD-FINE Hypodermic Needles — 206 UDI-DI variants, MDR

MD Atlas
KD Medical GmbH Hospital Products

Data from EUDAMED, last updated May 23, 2026

KD-FINE Hypodermic Needles

4031881G10-01IIaKB

206 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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 4031881G10-01IIaKB
Device name: KD-FINE Hypodermic Needles
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 1, 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

206 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KN3TYHRWJ9KKBESSYRFFXTBB

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

911501B74031881911500
911648E44031881911646
912454B74031881912453
911846B74031881911845
911495B74031881911494
911761E44031881911769
911815B74031881911814
911600S14031881911607
911778E44031881911776
911501S14031881911508
911792B74031881911791
911693B74031881911692
911662B74031881911661
911525B74031881911524
911594S14031881911591
911754E44031881911752
911617B74031881911616
911907B74031881911906
911907S14031881911904
911884S14031881911881
911709S14031881911706
911723S14031881911720
911686B74031881911685
911754S14031881911751
911884B74031881911883

5 6 7 8 9