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Achilles

EUDAMED

Class IIa (EU MDR)

Ref 804-060040-040

by BrosMed Medical Co., Ltd

Identity

Trade Name
Achilles EUDAMED
Device Name
Achilles PTA Balloon Dilatation Catheter EUDAMED
Model / Reference
804-060040-040 EUDAMED

Identifiers

Primary DI / UDI-DI
06958481458275 EUDAMED
Basic UDI-DI
695848140014M2 EUDAMED
B-06958481458275 EUDAMED
EMDN Code
C010402020101 PTA BALLOON DILATATION CATHETERS 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

Category: Peripheral angioplasty balloon catheter, basic

Achilles by BrosMed Medical Co., Ltd. — Class IIa — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral angioplasty balloon catheter, basic.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

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Manufacturer

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

Sources (2)

  • EUDAMED 0a9fd67b-a301-4fe3-8a07-080d5937edc7 61 fields · synced Jul 10, 2026
  • EUDAMED bd1bb1b8-1a44-45b2-a3f9-94ee7be46ca1 61 fields · synced May 18, 2026