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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

1308490 — Class III MDR by Noventure S.L.U.

MD Atlas
Noventure S.L.U.

EUDAMED last updated this device on Jul 25, 2025

1308490

843659383TAS133M2

On the marketClass III

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Noventure S.L.U.
UDI-DI code: 08436593830090
Reference / catalog number: 1308490

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Manufacturer information

Organization name: Noventure S.L.U.
SRN: ES-MF-000000797
Manufacturer status: Active

Related devices

CYS-CONTROL ULTRAB-1313022UNOn the market 1291481843659383OLA923KZOn the market 1308500843659383TAS123LXOn the market 1308499843659383TAS133M2On the market 1308533843659383TAS133M2On 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.

Critical warnings

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

CW267
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Dec 1, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08436593830090
Basic UDI-DI: 843659383TAS133M2
Reference / catalog number: 1308490
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: 4 Bustine
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

G99GASTROINTESTINAL DEVICES - OTHER

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification