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HemoWeld-MC

EUDAMED

Class I (EU MDR)

Ref HWELD-MC.DB.00

by Delcon Srl

Identity

Trade Name
HemoWeld-MC EUDAMED
Device Name
Sealer EUDAMED
Model / Reference
HWELD-MC.DB.00 EUDAMED

Identifiers

Primary DI / UDI-DI
08033928530528 EUDAMED
Basic UDI-DI
803392853SEALFP EUDAMED
Direct Marketing DI
08033928530528 EUDAMED
EMDN Code
B0180 BLOOD BAGS AND KITS - ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

HemoWeld-MC by Delcon Srl — 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
Delcon Srl
EUDAMED SRN
IT-MF-000014234

Sources (1)

  • EUDAMED 08af6dcb-77fb-4a8c-8012-fb8de7696803 61 fields · synced Jun 19, 2026