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

570087 — Class I MDR by Laboratorios URGO S.L.

MD Atlas
Laboratorios URGO S.L.

EUDAMED last updated this device on Mar 16, 2026

570087

8413647EXTRAFUERTEFL

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Laboratorios URGO S.L.
UDI-DI code: 08413647700875
Reference / catalog number: 570087

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: Laboratorios URGO S.L.
SRN: ES-MF-000000629
Manufacturer status: Active

Critical warnings

5 warnings recorded — scroll inside the panel to see all entries.

CW999
Mantener fuera del alcance y la vista de los niños
CW999
Cerrar bien el tubo después de cada aplicación
CW999
Mantener la boca y el tapón del tubo secos
CW999
No usar en caso de hipersensibilidad a algunos de los ingredientes
CW999
No utilizar después de la fecha de caducidad indicada

Market distribution

Primary placement in Spain; available across 1 country total.

Placed on the market in Spain; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08413647700875
Basic UDI-DI: 8413647EXTRAFUERTEFL
Reference / catalog number: 570087
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: Crema adhesiva para prótesis dentales
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

P01020180DENTAL IMPLANTS - ACCESSORIES

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

Related devices

6042398413647ULTRAFUERTEL8On the market ES00037428413647ULTRASINSABORVZOn the market 6048438413647NF306SGOn the market ES00021918413647BENFIXU6On the market ES00036708413647ULTRASINSABORVZOn 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.