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Tempus LS

EUDAMED

Class IIb (EU MDR)

Ref 3.940590Model TEMPUS LS

by Schiller Ag

Identity

Trade Name
Tempus LS EUDAMED
Device Name
TEMPUS LS EUDAMED
Model / Reference
TEMPUS LS EUDAMED
3.940590 EUDAMED

Identifiers

Primary DI / UDI-DI
07613365001693 EUDAMED
Basic UDI-DI
B-07613365001693 EUDAMED
EMDN Code
Z12030503 AUTOMATIC DEFIBRILLATORS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Tempus LS by Schiller AG — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Schiller Ag
EUDAMED SRN
CH-MF-000012722
Authorised Representative
SCHILLER Medizintechnik GmbH DE-AR-000006934

Sources (1)

  • EUDAMED 86e932ef-d67c-4dd4-a988-fea88c2a0927 61 fields · synced Jun 18, 2026