Statistique de GE Healthcare Finland Oy

227Dispositifs total

90UDI-DI de base

0Non destinés au marché UE

1Certificats

1Valides

0Expirant < 6 mois

1Pays

Santé des certificats de GE Healthcare Finland Oy

Affichage de 126–150 sur 227 dispositifs.

Dénomination commerciale	Numéro de référence/catalogue	Code d'UDI-DI	Quantité	Statut
5876727	`5876727`	`00195278522320`	1	Sur le marché
2104107-002	`2104107-002`	`00840682136365`	1	Sur le marché
2104166-004	`2104166-004`	`00840682136570`	1	Sur le marché
2104166-001	`2104166-001`	`00840682136488`	1	Sur le marché
2104162-002	`2104162-002`	`00840682136549`	1	Sur le marché
2104166-002	`2104166-002`	`00840682136358`	1	Sur le marché
2104166-003	`2104166-003`	`00840682136396`	1	Sur le marché
2104162-004	`2104162-004`	`00840682136525`	1	Sur le marché
2104162-003	`2104162-003`	`00840682136327`	1	Sur le marché
2104158-004	`2104158-004`	`00840682136501`	1	Sur le marché
2104107-003	`2104107-003`	`00840682136587`	1	Sur le marché
2103966-001	`2103966-001`	`00840682136341`	1	Sur le marché
2104158-003	`2104158-003`	`00840682136334`	1	Sur le marché
2104158-001	`2104158-001`	`00840682136518`	1	Sur le marché
2104162-001	`2104162-001`	`00840682136457`	1	Sur le marché
2104158-002	`2104158-002`	`00840682136556`	1	Sur le marché
2104107-004	`2104107-004`	`00840682136464`	1	Sur le marché
M1174413	`M1174413`	`00840682102971`	1	Sur le marché
TS-F4-GE	`TS-F4-GE`	`00840682103435`	1	Sur le marché
TS-F-D	`TS-F-D`	`00840682103206`	1	Sur le marché
M1115512	`M1115512`	`00840682103992`	1	Sur le marché
E-PiCCO-00	`E-PiCCO-00`	`00840682104036`	1	Sur le marché
57268-HEL	`57268-HEL`	`00840682103633`	1	Sur le marché
M1050784	`M1050784`	`00840682102964`	1	Sur le marché
TS-E-D	`TS-E-D`	`00840682103251`	1	Sur le marché

Dispositifs placés dans 1 pays

Mise à jour EUDAMED : le 25 mai 2026

FI-MF-000001176

Actif

Nom: Finnish Medicines Agency, Supervision and licences, Medical Device Unit
SRN: FI-CA-006
Téléphone: +358 29 522 3341
Email: registry@fimea.fi

PÄIVINEN Tarja
(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 EU MDR Article 10(10); (d) The reporting obligations referred to in EU MDR Articles 87 to 91 are fulfilled
Masqué
SALMENKAITA Mari
(b) The technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; (e) Investigational devices conform to the general safety and performance requirements apart from the aspects covered by the clinical investigation and that, with regard to those aspects, every precaution has been taken to protect the health and safety of the subject.
Masqué