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Schiller Medical

Active in EUDAMED

Francefrom SRN EUDAMED FDA SRN FR-MF-000003190 FEI 3002807785

Schiller Medical is a medical device manufacturer based in France, with 23 devices listed in FDA GUDID and EUDAMED (FDA Class II; EU Class IIb) as of 12 Nov 2026.

Devices
23
Registrations
EUDAMEDFDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA GUDID 13
  • EUDAMED 10

A device listed in two registries counts in both.

Device classes
  • FDA Class II 13
  • EU Class IIb 10
Identifiers
  • EUDAMED SRN FR-MF-000003190
  • FDA FEI 3002807785
  • DUNS 264351388

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI

Catalogue23

Newest first, rows 1-23 of 23

Search and filter all 23 devices
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  • Schiller Ref 1-128-9900

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb
  • Schiller Ref 1-127-9902

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb
  • SCHILLER SpO2 sensor Y 4, 2m

    Active Regimes: 510(k) Registry: GUDID Class:II
  • SCHILLER SpO2 sensor Y 5, 5m

    Active Regimes: 510(k) Registry: GUDID Class:II
  • SCHILLER ECG patient cable type IV

    Active Regimes: 510(k) Registry: GUDID Class:II
  • SCHILLER SpO2 sensor Children

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Schiller

    Active Regimes: 510(k) Registry: GUDID Class:II
  • SCHILLER SpO2 Sensor wireless

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Schiller

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Schiller

    Active Regimes: 510(k) Registry: GUDID Class:II
  • SCHILLER MAGLIFE Serenity

    Active Regimes: 510(k) Registry: GUDID Class:II
  • SCHILLER Temp. Probe optical skin

    Active Regimes: 510(k) Registry: GUDID Class:II
  • SCHILLER MAGSCREEN Serenity

    Active Regimes: 510(k) Registry: GUDID Class:II
  • SCHILLER ECG sensor type IV

    Active Regimes: 510(k) Registry: GUDID Class:II
  • SCHILLER SpO2 sensor Adult

    Active Regimes: CE MDD 510(k) Registry: GUDID Class:II
  • Schiller Ref 1-58-9501

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb
  • Schiller Ref 1-58-9502

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb
  • Schiller Ref 1-130-9816

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb
  • Schiller Ref 1-131-9903

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb
  • Schiller Ref 1-108-9902

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb
  • Schiller Ref 1-58-9100

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb
  • Schiller Ref 1-58-9901

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb
  • Schiller Ref 1-127-9901

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb

Rows 1-23 of 23

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
FR-MF-000003190
FDA FEI number
3002807785
DUNS number
264351388
EU VAT number
FR29310967294
EUDAMED status
Active
EUDAMED registered name
SCHILLER MEDICAL
Registered address
4, Louis Pasteur, 67160, Wissembourg, France
Phone
+33388633600
PRRC contact
Jean-Philippe Didon(public in EUDAMED)

Frequently asked questions

How many devices does SCHILLER MEDICAL have in the registry?

The registry currently lists 23 devices for SCHILLER MEDICAL. Devices recorded under merged duplicate company entries are counted once.

Which registries list SCHILLER MEDICAL's devices?

Among its 23 most recently registered devices, SCHILLER MEDICAL has devices listed in EUDAMED (10 devices) and FDA GUDID (13 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do SCHILLER MEDICAL's devices fall under?

Among its 23 most recently registered devices, the classes recorded for SCHILLER MEDICAL's devices are Class IIb and Class II. Each device page shows its own class and authorisation.

What are the newest devices from SCHILLER MEDICAL in the registry?

The most recently registered devices listed for SCHILLER MEDICAL include SCHILLER, SCHILLER SpO2 sensor Y 4,2m, SCHILLER SpO2 sensor Y 5,5m and SCHILLER ECG patient cable type IV.

Generated automatically from registry data and not verified by a human reviewer.