← Back to catalogue

Heka Soft

EUDAMED

Class I (EU MDR)

Ref NK0720

by Allion BV h.o.d.n. van Heek Medical

Identity

Trade Name
Heka Soft EUDAMED
Device Name
Non-woven swab EUDAMED
Model / Reference
NK0720 EUDAMED

Identifiers

Primary DI / UDI-DI
08715886000472 EUDAMED
Basic UDI-DI
8715886NonWovenKompresKM EUDAMED
EMDN Code
M0202010102 NON-WOVEN FOLDED GAUZES, WITHOUT X-RAY DETECTABLE THREAD, NON-STERILE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Heka Soft by Allion BV h.o.d.n. van Heek Medical — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
NL-MF-000003490

Sources (1)

  • EUDAMED a69ecc7a-a1ce-4fd6-a458-d2aaf9fde5b3 61 fields · synced Jun 19, 2026