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body fluid solidification gel

EUDAMED

Class I (EU MDR)

Ref 9830-200

by Vacsax Limited

Identity

Device Name
body fluid solidification gel EUDAMED
Model / Reference
9830-200 EUDAMED

Identifiers

Primary DI / UDI-DI
05055761600179 EUDAMED
Basic UDI-DI
505576166294736 EUDAMED
Unit of Use DI
05055761602852 EUDAMED
EMDN Code
A0680 DRAINAGE AND FLUID COLLECTION DEVICES - ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland 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

body fluid solidification gel by Vacsax Limited — 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
Vacsax Limited
EUDAMED SRN
GB-MF-000003621
Authorised Representative
Fannin Ltd. IE-AR-000002249

Sources (1)

  • EUDAMED 2c6ae09c-fcac-4d3e-8e16-b6686f0aab5b 61 fields · synced Jun 17, 2026