Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ 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.

Organization name
UDI-DI code
Reference / catalog number

5999577910001 — IVDR Class A IVDR by DiagnostIQ Korlátolt…

MD Atlas
DiagnostIQ Korlátolt Felelősségű Társaság

EUDAMED last updated this device on Mar 19, 2025

5999577910001

599957791SMRBASIC1S7

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: DiagnostIQ Korlátolt Felelősségű Társaság
UDI-DI code: 05999577910001
Reference / catalog number: 5999577910001

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?

Manufacturer information

Organization name: DiagnostIQ Korlátolt Felelősségű Társaság
SRN: HU-MF-000046944
Manufacturer status: Active

Market distribution

Primary placement in Hungary; available across 1 country total.

Country	On market since	Until
HungaryPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05999577910001
Basic UDI-DI: 599957791SMRBASIC1S7
Reference / catalog number: 5999577910001
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W02069092VARIOUS SAMPLE PROCESSING INSTRUMENTS - IVD MEDICAL DEVICE SOFTWARE

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

5999577910032599957791SMRNORMAL12ZOn the market 5999577910063599957791SMRTHYRB16MOn the market 5999577910100599957791SMRTHEXT001XNOn the market 5999577910094599957791SMRTHPRE001WSOn the market 5999577910049599957791SMRPREM1DGOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.