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Apollo Balloon Dilatation Catheters

EUDAMED

Class III (EU MDR)

Ref 802-5006

by BrosMed Medical Co., Ltd

Identity

Device Name
Apollo Balloon Dilatation Catheters EUDAMED
Model / Reference
802-5006 EUDAMED

Identifiers

Primary DI / UDI-DI
06958481455519 EUDAMED
Basic UDI-DI
B-06958481455519 EUDAMED
EMDN Code
C010401020101 PTCA BALLOON DILATION CATHETERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Coronary angioplasty balloon catheter, cutting/scoring

Apollo Balloon Dilatation Catheters by BrosMed Medical Co., Ltd. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Coronary angioplasty balloon catheter, cutting/scoring.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

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

Sources (1)

  • EUDAMED 2064a432-2f2d-409d-98c2-d3bd9477a6f2 61 fields · synced May 22, 2026