Statistique de Tcoag ireland ltd

64Dispositifs total

64UDI-DI de base

0Non destinés au marché UE

0Certificats

0Valides

0Expirant < 6 mois

10Pays

Santé des certificats de Tcoag ireland ltd

Aucun certificat enregistré pour ce fabricant.

Dispositifs par classe de risque

Catalogue des dispositifs de Tcoag ireland ltd

Affichage de 51–64 sur 64 dispositifs.

Dénomination commerciale	Numéro de référence/catalogue	Code d'UDI-DI	Quantité	Statut
TriniCLOT Fibrinogen Kit	`T1301`	`05391521420350`	1	Sur le marché
TriniCLOT Imidazole Buffer	`T1901`	`05391521420503`	1	Sur le marché
TriniCLOT Imidazole Buffer	`T1901`	`05391521420503`	1	Sur le marché
TriniCLOT Lupus Confirm	`T1605`	`05391521420480`	1	Sur le marché
TriniCLOT Owrens Buffer	`T1903`	`05391521421210`	1	Sur le marché
TriniCLOT PC II	`T1607`	`05391521421197`	1	Sur le marché
TriniCLOT PS II	`T1608`	`05391521421203`	1	Sur le marché
TriniCLOT PT Excel S 20 mL	`T1103`	`05391521420251`	1	Sur le marché
TriniCLOT PT Excel S 6ml	`T1104`	`05391521420268`	1	Sur le marché
TriniCLOT Thrombin Time 1ml	`T1411`	`05391521420817`	1	Sur le marché
TriniCLOT Thrombin Time 4ml	`T1414`	`05391521420824`	1	Sur le marché
TriniLIA D-dimer	`T3101`	`05391521420572`	1	Sur le marché
TriniLIA D-Dimer II	`T3104`	`05391521421494`	1	Sur le marché
W0103020606	`T1604`	`05391521420473`	1	Sur le marché

1 2 3

Présence sur le marché de Tcoag ireland ltd

Dispositifs placés dans 10 pays

France14
Irlande13
Allemagne12
Autriche9
Belgique7
Finlande3
Espagne2
Pays-Bas2
Danemark1
Italie1

Mise à jour EUDAMED : le 2 juil. 2024

Tcoag ireland ltd

IE-MF-000027371

Actif

Adresse: IDA Business Park, Southern Cross Road, A98 X383 Co. Wicklow
Rôle: Fabricant
Date d'enregistrement: 15 août 2022
Pays: IE Ireland

Information sur Tcoag ireland ltd

SRN: IE-MF-000027371
Rôle: Fabricant
Pays: Irlande
Nom de l'organisation: Tcoag ireland ltd
Numéro TVA UE: IE9742077F
EORI: IE9742077F
Registre du commerce: 482053
Date d'enregistrement: 15 août 2022

Contact de Tcoag ireland ltd

Adresse: IDA BUSINESS PARK, SOUTHERN CROSS ROAD BRAY A98 X383 CO. WICKLOW IRLANDE
Téléphone: 00353 1 2746614
Email: Pauline.McManus@tcoag.com
Site web: https://www.tcoag.com

Autorité compétente

Nom: Health Products Regulatory Authority, Medical Devices Department
SRN: IE-CA-001
Téléphone: +353 1 676 4971
Email: devices@hpra.ie

Dirigeants et représentants réglementaires de Tcoag ireland ltd

MCMANUS Pauline
(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; (b) the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; (c) the post-market surveillance obligations are complied with (d) the reporting vigilance obligations are fulfilled; (e) performance studies referred to in Section 4.1 of Annex XIV
Masqué
PRENDERGAST Paula
Regulatory activities: (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; (b) the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; (c) the post-market surveillance obligations are complied with (d) the reporting vigilance obligations are fulfilled; (e) performance studies referred to in Section 4.1 of Annex XIV
Masqué
MCDONALD Tom
Quality Assurance activities: (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; (b) the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; (c) the post-market surveillance obligations are complied with (d) the reporting vigilance obligations are fulfilled; (e) performance studies referred to in Section 4.1 of Annex XIV
Masqué