Statistique de Galena Pharma Oy

79Dispositifs total

58UDI-DI de base

0Non destinés au marché UE

1Certificats

1Valides

0Expirant < 6 mois

5Pays

Santé des certificats de Galena Pharma Oy

Affichage de 26–50 sur 79 dispositifs.

Dénomination commerciale	Numéro de référence/catalogue	Code d'UDI-DI	Quantité	Statut
Galax enema 2x5ml	`350179`	`06420615710790`	1	Sur le marché
Galax enema 4x5ml	`350179`	`06420615710806`	1	Sur le marché
503007	`503007`	`D-503007MT`	1	Sur le marché
503008	`503008`	`D-503008MV`	1	Sur le marché
350143/665001	`350143/665001`	`06420615711001`	1	Sur le marché
321896	`321896`	`06430020731440`	1	Sur le marché
Mobilat Ice Strong 75 ml roll on	`350138`	`06430030150071`	1	Sur le marché
745021	`745021`	`06420615711179`	1	Sur le marché
Multi-Gyn HydraCream + applicator 50g	`725125/484002`	`06420615710899`	1	Sur le marché
Multi-Gyn HydraCream 25g	`350193/484001`	`06420615710875`	1	Sur le marché
Multi-Gyn HydraCream 50g	`350193/350226`	`06420615710882`	1	Sur le marché
3028	`3028`	`06430020483028`	1	Sur le marché
3011	`3011`	`06430020483011`	1	Sur le marché
684001	`684001`	`06420615710776`	1	Sur le marché
340044	`340044`	`06420615710783`	1	Sur le marché
473011	`473011`	`06420615710646`	1	Sur le marché
473010	`473010`	`06420615710639`	1	Sur le marché
Radian Ice 150 ml	`350138`	`06430030150057`	1	Sur le marché
Radian Ice 75 ml roll-on	`350138`	`06430030150040`	1	Sur le marché
Radian Ice cold gel 150 ml	`745012`	`06420615711124`	1	Sur le marché
Radian Ice cold gel 50 ml	`745009`	`06420615711155`	1	Sur le marché
Radian Ice cold gel 75 ml	`745011`	`06420615711117`	1	Sur le marché
Refenum Ice 150 ml	`350138`	`06430030150002`	1	Sur le marché
Refenum Ice 50 ml	`350138`	`06430030150101`	1	Sur le marché
745010	`745010`	`06420615711162`	1	Sur le marché

Dispositifs placés dans 5 pays

Mise à jour EUDAMED : le 3 mars 2026

FI-MF-000000588

Actif

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

MAUNU Piritta
(b) the technical documentation and the EU DoC are drawn up and kept up-to-date;(c) the PMS obligations are complied ref. Art. 10(10);(d) the reporting obligations ref. to in Art. 87 to 91 are fulfilled; ref. to vigilance reporting.(e) in the case of investigational devices, the statement ref. to Annex XV. Deputy:(a) the conformity of the devices is appr. checked, in accordance with the QMS under which the devices are manufactured, before releasing.
Masqué
HEIKKINEN Inka
(a) the conformity of the devices is appr. checked, in accordance with the QMS under which the devices are manufactured, before releasing. Deputy: (b) the technical documentation and the EU DoC are drawn up and kept up-to-date;(c) the PMS obligations are complied ref. Art. 10(10);(d) the reporting obligations ref. to in Art. 87 to 91 are fulfilled; ref. to vigilance reporting.(e) in the case of investigational devices, the statement ref. to Annex XV.
Masqué