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Bulkamid® Needle

EUDAMED

Class IIa (EU MDR)

Ref 10001491

by Contura International A/S

Identity

Trade Name
Bulkamid® Needle EUDAMED
Device Name
Bulkamid® Needle EUDAMED
Model / Reference
10001491 EUDAMED

Identifiers

Primary DI / UDI-DI
05704101014915 EUDAMED
Basic UDI-DI
5704101BUNEWY EUDAMED
EMDN Code
U0780 DEVICES FOR THE TREATMENT OF INCONTINENCE - ACCESSORIES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

Yes

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

Bulkamid® Needle by Contura International A/S — Class IIa — 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
DK-MF-000002018

Sources (1)

  • EUDAMED 808214fe-5536-43ec-8a6e-cac3899fdd45 61 fields · synced Oct 5, 2026