Statistique de CYTOGNOS, S.L

42Dispositifs total

41UDI-DI de base

0Non destinés au marché UE

0Certificats

0Valides

0Expirant < 6 mois

1Pays

Santé des certificats de CYTOGNOS, S.L

Aucun certificat enregistré pour ce fabricant.

Affichage de 26–42 sur 42 dispositifs.

Dénomination commerciale	Numéro de référence/catalogue	Code d'UDI-DI	Quantité	Statut
Kappa-FITC/Lambda-PE	`CYT-KF2-LPE-100`	`08436548980948`	1	Sur le marché
Kappa-PE	`CYT-KAPPPE2`	`08436548983772`	1	Sur le marché
KAPPA-PE	`CYT-KAPPPE`	`08436548980924`	1	Sur le marché
Lambda-APC-C750	`CYT-LAC750-2`	`08436548983802`	1	Sur le marché
LAMBDA-APC-C750	`CYT-LAC750`	`08436548980979`	1	Sur le marché
Lambda-FITC	`CYT-LAMBF2`	`08436548983796`	1	Sur le marché
LAMBDA-FITC	`CYT-LAMBF`	`08436548980986`	1	Sur le marché
Lambda-FITC/Kappa-PE	`CYT-LF-KPE-100`	`08436548981037`	1	Sur le marché
Lambda-PE	`CYT-LAMBPE2`	`08436548983758`	1	Sur le marché
LAMBDA-PE	`CYT-LAMBPE`	`08436548980993`	1	Sur le marché
Lymphoid Screening Tube (LST)	`CYT-LST`	`08436548981563`	1	Sur le marché
Multiple Mieloma Minimal Residual Disease	`CYT-MM-MRD8`	`08436548983673`	1	Sur le marché
Primary Immunodeficiency Orientation Tube (PIDOT)	`CYT-PIDOT8`	`08436548983703`	1	Sur le marché
CYT-QL-1	`CYT-QL-1`	`08436548981075`	1	Sur le marché
CYT-QL-3	`CYT-QL-3`	`08436548981099`	1	Sur le marché
Small Sample Tube (SST)	`CYT-SST`	`08436548981112`	1	Sur le marché
TCRgammadelta-PE-Cyanine7	`CYT-TCRGDPECY7`	`08436548982775`	1	Sur le marché

Dispositifs placés dans 1 pays

Mise à jour EUDAMED : le 2 mai 2024

ES-MF-000000318

Actif

Adresse: Carretera de Madrid Km. 0, Poligono La Serna, Nave 9, 37900 Santa Marta de Tormes
Rôle: Fabricant
Date d'enregistrement: 17 déc. 2020
Pays: ES Spain

Adresse: CARRETERA DE MADRID KM. 0, POLIGONO LA SERNA, NAVE 9 37900 SANTA MARTA DE TORMES ESPAGNE
Téléphone: +34 923125067
Email: direction@cytognos.com
Site web: www.cytognos.com

RODRÍGUEZ CORCHETE Lorena
The PRRC’s is responsible for ensuring that: a) the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released; c) the post-market surveillance obligations are complied with in accordance with Article 10(9); d) the reporting obligations referred to in Articles 82 to 86 are fulfilled;
Masqué
HERNANDEZ GALANTE Henar
The PRRC’s is responsible for ensuring that: b) the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; e) in the case of devices for performance studies intended to be used in the context of interventional clinical performance studies or other performance studies involving risks for the subjects, the statement referred to in Section 4.1 of Annex XIV is issued.
Masqué