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Spirette FA Pro/LAB (basic unit)

EUDAMED

Class I (EU MDR)

Ref 2050-70

by NDD Medizintechnik AG

Identity

Trade Name
Spirette FA Pro/LAB (basic unit) EUDAMED
Device Name
Breathing tubes EUDAMED
Model / Reference
2050-70 EUDAMED

Identifiers

Primary DI / UDI-DI
07640142190646 EUDAMED
Basic UDI-DI
764014219BreathingTubes6L EUDAMED
EMDN Code
Z12150185 SPIROMETRY 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

Category: Pulmonary function testing filter/mouthpiece

Spirette FA Pro/LAB (basic unit) by NDD Medizintechnik AG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary function testing filter/mouthpiece.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CH-MF-000015550
Authorised Representative
NDD Medizintechnik GmbH DE-AR-000032322

Sources (1)

  • EUDAMED 40907237-259b-4dae-92f1-b8308c748fdb 61 fields · synced Jul 9, 2026