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TransFix

EUDAMED

Class I (EU MDR)

Ref HSOTRFIX4000

by MSP Medizintechnik GmbH

Identity

Trade Name
TransFix EUDAMED
Device Name
TransFix EUDAMED
Model / Reference
HSOTRFIX4000 EUDAMED

Identifiers

Primary DI / UDI-DI
09120047880371 EUDAMED
Basic UDI-DI
912004788HSOTRFIXAC EUDAMED
EMDN Code
R9080 RESPIRATORY AND ANESTHESIA DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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: Gas-sampling/monitoring respiratory tubing, single-use

TransFix by MSP Medizintechnik GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Gas-sampling/monitoring respiratory tubing, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union No Longer Active

CE/MDR

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Manufacturer

EUDAMED SRN
AT-MF-000018341

Sources (1)

  • EUDAMED 2f45c0c9-e52d-4dcf-95e8-29c80ca52859 61 fields · synced Jul 27, 2026