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SentrySuite 3.30

EUDAMED

Class IIa (EU MDR)

Ref V-770968

by Jaeger Medical GmbH

Identity

Device Name
SentrySuite 3.30 EUDAMED
Model / Reference
V-770968 EUDAMED

Identifiers

Primary DI / UDI-DI
04250892907345 EUDAMED
Basic UDI-DI
42508929012112AG3 EUDAMED
Direct Marketing DI
04250892907345 EUDAMED
EMDN Code
Z12159082 VARIOUS PNEUMOLOGY AND RESPIRATORY PHYSIOPATHOLOGY INSTRUMENTS - SOFTWARE ACCESSORIES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

SentrySuite 3.30 by Jaeger Medical GmbH — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Jaeger Medical GmbH
EUDAMED SRN
DE-MF-000007090

Sources (1)

  • EUDAMED a2e8f992-a81f-4762-b9cb-048583968329 61 fields · synced Jun 19, 2026