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.

DOCTORS KIT DKS 2521-25 — 1 UDI-DI variant, IVDD

MD Atlas
Eldon Biologicals A/S

Data from EUDAMED, last updated May 31, 2026

DOCTORS KIT DKS 2521-25

B-05713494002003

1 UDI-DI variant

IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]IVDD — Annex II List A

Legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk class: IVDD — Annex II List A
Manufacturer: Eldon Biologicals A/S

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

ReagentNear-patient testingProfessional testingHuman tissues / cellsAnimal tissues / cells

Legacy certificates

Certificate number: DGM-491
Type: refdata.legacy.ivdd-certificate-type.v
Notified body: Presafe Denmark A/S (0543)
Validity: May 26, 2024

Certificate number: DGM-492
Type: refdata.legacy.ivdd-certificate-type.vii-5
Notified body: Presafe Denmark A/S (0543)
Validity: Dec 18, 2023

Identity & classification

Basic UDI-DI: B-05713494002003
Device name: DOCTORS KIT DKS 2521-25
Device model: 610-13v05
Issuing agency: EUDAMED
Legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk class: IVDD — Annex II List A
Version date: Nov 22, 2023

Manufacturer & authorised representative

Manufacturer

Name: Eldon Biologicals A/S
SRN: DK-MF-000025470
Country: Denmark
Email: eldoncard@eldoncard.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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

basicUdiUlid01HFT3Z14RZRQK1TMW3WQCDN2X

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

DOCTORS KIT DKS 2521-2505713494002003