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ARGUS PRO LifeCare 2
EUDAMEDClass IIb (EU MDR)
Ref 3.940543Model ARGUS PRO LifeCare 2 - APLC2 GSM-version
by Schiller Ag
Identity
- Trade Name
- ARGUS PRO LifeCare 2 EUDAMED
- Device Name
- ARGUS PRO LifeCare 2 EUDAMED
- Model / Reference
- ARGUS PRO LifeCare 2 - APLC2 GSM-version EUDAMED3.940543 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07613365001419 EUDAMED
- Basic UDI-DI
- B-07613365001419 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
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
ARGUS PRO LifeCare 2 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-07613365001419 | Class IIb | Active |
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Manufacturer
- Manufacturer
- Schiller Ag
- EUDAMED SRN
- CH-MF-000012722
- Authorised Representative
- SCHILLER Medizintechnik GmbH DE-AR-000006934
Sources (1)
- EUDAMED 4f76d94c-3869-404d-b72c-68f7d0bb1ae3 61 fields · synced Jul 11, 2026