Pricing Sign in

Role
Country
Date of registration
Address

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.

Organization name
UDI-DI code
Reference / catalog number

wersja wtryskowa zasilana ciekłym… — Class IIa MDR

MD Atlas
Maximus s.c. Robert Klejdysz, Alicja Daniecka-Klejdysz

EUDAMED last updated this device on Feb 27, 2026

wersja wtryskowa zasilana ciekłym azotem

59046735579MX-4CPK6

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Maximus s.c. Robert Klejdysz, Alicja Daniecka-Klejdysz
UDI-DI code: 05904673557920
Reference / catalog number: wersja wtryskowa zasilana ciekłym azotem

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?

View device family (Basic UDI)

Manufacturer information

Organization name: Maximus s.c. Robert Klejdysz, Alicja Daniecka-Klejdysz
SRN: PL-MF-000045281
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in Poland; available across 1 country total.

Country	On market since	Until
PolandPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05904673557920
Basic UDI-DI: 59046735579MX-4CPK6
Reference / catalog number: wersja wtryskowa zasilana ciekłym azotem
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://www.kriokomora.com/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05904673557920

Sign in to download the DataMatrix

Create a free account to download the UDI-DI DataMatrix for this device.

Email

Password

No account yet?

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

Sign in to generate the UDI-PI DataMatrix

Create a free account, then generate the compliant UDI-PI carrier for this device.

Email

Password

No account yet?

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z12069003CRYOTHERAPY CHAMBERS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

Become a partner of MD Atlas

Related devices

wersja wymiennikowa59046735579MX-4CPK6On the market wersja wtryskowa zasilana ciekłym powietrzem59046735579MX-4CPK6On the market CARGO MX-35908047599wozekdobutli8VOn the market Sani MX-O359046735579MX-O3B6On the market BLUE AIR MX-259046735579MX289On the market

Certificates

Certificate health across this manufacturer's portfolio.

1434-MDR-023/2024Issued
Quality assuranceNotified body: 1434Expiry: Jan 8, 2030