Statistics for GE Healthcare Finland Oy

227Total Devices

90Basic UDI-DIs

0Not destined for EU market

1Certificates

1Valid

0Expiring < 6 months

1Countries

Certificate health for GE Healthcare Finland Oy

Showing 76–100 of 227 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
2106307-001	`2106307-001`	`00840682137836`	1	On the market
N-EEGX	`N-EEGX`	`00840682125635`	1	On the market
2106389-005	`2106389-005`	`00840682139786`	1	On the market
2106390-001	`2106390-001`	`00840682139687`	1	On the market
2106307-003	`2106307-003`	`00840682137744`	1	On the market
2106389-004	`2106389-004`	`00840682140089`	1	On the market
2106390-002	`2106390-002`	`00840682140232`	1	On the market
2106389-002	`2106389-002`	`00840682139779`	1	On the market
2106389-001	`2106389-001`	`00840682139960`	1	On the market
2106389-003	`2106389-003`	`00840682139700`	1	On the market
2106383-006	`2106383-006`	`00840682139816`	1	On the market
2106383-004	`2106383-004`	`00840682140171`	1	On the market
2106385-001	`2106385-001`	`00840682139588`	1	On the market
2106383-005	`2106383-005`	`00840682140034`	1	On the market
2106383-003	`2106383-003`	`00840682139618`	1	On the market
2106307-004	`2106307-004`	`00840682137874`	1	On the market
2106381-004	`2106381-004`	`00840682139939`	1	On the market
2106383-002	`2106383-002`	`00840682140096`	1	On the market
2106381-005	`2106381-005`	`00840682139854`	1	On the market
E-NSATX-00	`E-NSATX-00`	`00840682104265`	1	On the market
2106381-003	`2106381-003`	`00840682139847`	1	On the market
2106381-001	`2106381-001`	`00840682139953`	1	On the market
2106403-003	`2106403-003`	`00840682140430`	1	On the market
2106403-001	`2106403-001`	`00840682140157`	1	On the market
2104178-002	`2104178-002`	`00840682181907`	1	On the market

Devices placed in 1 country

EUDAMED update: May 25, 2026

FI-MF-000001176

Active

Name: Finnish Medicines Agency, Supervision and licences, Medical Device Unit
SRN: FI-CA-006
Phone: +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
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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.
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