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

FASTIDIOUS ANAEROBE AGAR — IVDR Class A IVDR by Sundial Co. Ltd

MD Atlas
Sundial Co. Ltd

EUDAMED last updated this device on Mar 31, 2026

FASTIDIOUS ANAEROBE AGAR

5298004040374YK

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Sundial Co. Ltd
UDI-DI code: 05298004040374
Reference / catalog number: SUN90720

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: Sundial Co. Ltd
SRN: CY-MF-000023765
Manufacturer status: Active

Related devices

ALKALINE PEPTONE WATER5298004040282YDOn the market BILE ESCULIN AGAR5298004040329YEOn the market BISMUTH SULPHITE/ SALMONELLA-SHIGELLA AGAR5298004040435YEOn the market BLOOD W/5% H.B / MACCONKEY W/C.V. AGAR5298004040381YGOn the market BLOOD W/5% H.B. / UTI AGAR5298004040190Y7On the market

Critical warnings

4 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.
CW007
EUDAMED did not publish a description for this code.
CW032
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Cyprus; available across 1 country total.

Country	On market since	Until
CyprusPrimary placement	Nov 14, 2016	Still on market

Device identification

Trade name: FASTIDIOUS ANAEROBE AGAR
UDI-DI code: 05298004040374
Basic UDI-DI: 5298004040374YK
Reference / catalog number: SUN90720
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)

W0104010405NON-CHROMOGENIC MEDIA (PLATES)

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

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.