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

911617S14031881911614
911556S14031881911553
911716S14031881911713
912393S14031881912390
911891S14031881911898
911778S14031881911775
912478B74031881912477
911891B74031881911890
911815E44031881911813
911822E44031881911820
912430E44031881912438
911679B74031881911678
911662E44031881911660
911648B74031881911647
911655E44031881911653
911532S14031881911539
911556E44031881911554
911761S14031881911768
911747E44031881911745
911723E44031881911721
911594B74031881911593
912478E44031881912476
911730S14031881911737
911822S14031881911829
911594E44031881911592

3 4 5 6 7