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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

ML13207 — Class I MDR by Internacional Ventur S.A.

MD Atlas
Internacional Ventur S.A.

EUDAMED last updated this device on Sep 4, 2023

ML13207

843702233600132EF

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Internacional Ventur S.A.
UDI-DI code: 08437022336770
Reference / catalog number: ML13207

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Manufacturer information

Organization name: Internacional Ventur S.A.
SRN: ES-MF-000000386
Manufacturer status: Active

Related devices

ML13206843702233600132EFOn the market VE13207843702233600132EFOn the market ML13211843702233600132EFOn the market ML13212843702233600132EFOn the market ML13202843702233600132EFOn the market

Market distribution

Primary placement in Spain; available across 2 countries total.

Country	On market since	Until
SpainPrimary placement		Still on market
Portugal		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08437022336770
Basic UDI-DI: 843702233600132EF
Reference / catalog number: ML13207
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Bolsas autosellantes para esterilización, de gran resistencia y calidad. Fabricadas con una capa de papel y otra de plástico para la visualización del contenido. Aptos para autoclaves de vapor o químicos. Incorpora un testigo de esterilización para la verificación del proceso.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

S01010101STERILISATION POUCHES, FLAT, PAPER/PLASTIC FILM

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

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.