Aperi NC

by BrosMed Medical Co., Ltd 45 variants

Ref 445030

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDD	NumberB-06958481486995 Basic UDI-DI 06958481486995UDI-DI	Date21 Dec 2021Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name: Aperi NC Balloon Dilatation Catheters
Model / Reference: 445030

Primary DI / UDI-DI: 06958481486995
Basic UDI-DI: B-06958481486995
EMDN Code: C010401020101 Ptca balloon dilation catheters

Device Class: Class III
EU market of registration: Netherlands

Manufacturer details

EUDAMED SRN: CN-MF-000007501
Authorised representative: Brosmed Medical B.V. NL-AR-000002616

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Properties

Sterile

Other properties (10)

Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No