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

Urea — IVDR Class A IVDR by VIAMAR INTERNATIONAL,…

MD Atlas
VIAMAR INTERNATIONAL, s.r.o.

EUDAMED last updated this device on Jan 9, 2026

Urea

85941999298307C6

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: VIAMAR INTERNATIONAL, s.r.o.
UDI-DI code: 08594199921885
Reference / catalog number: 98307-10

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: VIAMAR INTERNATIONAL, s.r.o.
SRN: CZ-MF-000038013
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Czechia; available across 1 country total.

Country	On market since	Until
CzechiaPrimary placement		Still on market

Device identification

Trade name: Urea
UDI-DI code: 08594199921885
Basic UDI-DI: 85941999298307C6
Reference / catalog number: 98307-10
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: 10
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)

W0104010206MEDIA IN TUBES (SOLID & LIQUID)

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

Alkaline peptone water 5ml85941999298115BTOn the market Antimycotic Sensitivity Agar ( Casitone )85941999298055C2On the market B.E.A. (Bile Esculin Azide) Agar85941999298448CROn the market Bacillus subtilis broth85941999298086CDOn the market BHI broth 100 ml85941999298018BUOn 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.