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

VE33524 — Class I MDR by Internacional Ventur S.A.

MD Atlas
Internacional Ventur S.A.

EUDAMED last updated this device on Apr 17, 2026

VE33524

84370223363352PW

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Internacional Ventur S.A.
UDI-DI code: 08435665305351
Reference / catalog number: VE33524

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: 08435665305351
Basic UDI-DI: 84370223363352PW
Reference / catalog number: VE33524
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 Starline están fabricados en látex 100% natural. Nuestro guante proporciona una adecuada barrera protectora a la vez que cuenta con una excelente elasticidad que lo hace especialmente cómodo y resistente. Caracteristicas: · Sin polvo. · Ambidiestros. · Superficie ligeramente texturada. · Producto no reutilizable. Composición: · Fabricados en látex 100% natural. [ES]
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T010201LATEX 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