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APS Tube

EUDAMED

Class I (EU MDR)

Ref V-892080

by Jaeger Medical GmbH

Identity

Device Name
APS Tube EUDAMED
Model / Reference
V-892080 EUDAMED

Identifiers

Primary DI / UDI-DI
14250892907090 EUDAMED
Basic UDI-DI
42508929240311QS EUDAMED
EMDN Code
Z12159085 VARIOUS PNEUMOLOGY AND RESPIRATORY PHYSIOPATHOLOGY INSTRUMENTS - CONSUMABLES EUDAMED

Classification

Device Class
Class I 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

APS Tube by Jaeger Medical GmbH — Class I — 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 37be5a55-2542-4bc4-a35c-5cfabd31b34a 61 fields · synced Jul 9, 2026