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

ML33542 — Class I MDR by Internacional Ventur S.A.

MD Atlas
Internacional Ventur S.A.

EUDAMED last updated this device on May 23, 2022

ML33542

843702233600335EX

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Internacional Ventur S.A.
UDI-DI code: 08437022336015
Reference / catalog number: ML33542

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

Related devices

ML13206843702233600132EFOn the market ML13207843702233600132EFOn the market VE13207843702233600132EFOn the market ML13211843702233600132EFOn the market ML13212843702233600132EFOn 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.

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: 08437022336015
Basic UDI-DI: 843702233600335EX
Reference / catalog number: ML33542
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: Los guantes de nitrilo Medicaline están fabricados 100% en nitrilo, evitando reacciones alérgicas en usuarios o pacientes con intolerancia al látex. Además proporcionan una óptima protección de las manos durante la realización de exámenes, diagnósticos y terapias. El grosor en esta gama de guantes es de 3 gramos, ofreciendo una mayor comodidad y una sensación de tacto más natural. Características: · No estériles. · Ambidiestros. · Color blanco, azul, violeta, rosa y negro. · Superficie microtexturada antideslizante. · Producto no reutilizable. Composición: Fabricados 100% en nitrilo.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T01020204NITRILE EXAMINATION / TREATMENT GLOVES

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