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Suction Unit Kits

EUDAMED

Class I (EU MDR)

Ref B03Ref B04

by Vega Technologies Inc.

Identity

Trade Name
Suction Unit Kits EUDAMED
Device Name
Suction Unit Kits EUDAMED
Model / Reference
B03 EUDAMED
B04 EUDAMED

Identifiers

Primary DI / UDI-DI
06946159504492 EUDAMED
06946159504751 EUDAMED
Basic UDI-DI
69461595BVC EUDAMED
EMDN Code
R05010399 MUCOSITY ASPIRATORS - OTHER 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

Suction Unit Kits by Vega Technologies Inc. — 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

EUDAMED SRN
CN-MF-000012927
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (2)

  • EUDAMED 7f4d6c8b-623b-48c1-8f99-7cbe83dc09e4 61 fields · synced Jul 28, 2026
  • EUDAMED 72d0493b-0ad3-46ea-97f9-777e977326cf 61 fields · synced May 18, 2026