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ASAHI Corsair Pro XS Microcatheter, 150cm

EUDAMEDFDA 510(k)

Class III (EU MDR)

Ref CSR150-21S

by Asahi Intecc Co., Ltd.

Identity

Trade Name
ASAHI Corsair Pro XS Microcatheter, 150cm EUDAMED
Device Name
ASAHI Corsair Pro XS Microcatheter, 150cm EUDAMED
Model / Reference
CSR150-21S EUDAMED

Identifiers

Primary DI / UDI-DI
04547327137836 EUDAMED
Basic UDI-DI
B-04547327137836 EUDAMED
EMDN Code
C0104010203 PHARMACEUTICAL INFUSION AND ADMINISTRATION INTRACORONARY AND INTRACARDIAC CATHETERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Austria 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

ASAHI Corsair Pro XS Microcatheter, 150cm by Asahi Intecc Co., Ltd. — Class III — FDA_510K, MDD — listed in EUDAMED, FDA 510(k) — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
JP-MF-000010199
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED a91f6d22-9f5d-4597-8d1c-fbcf9125a818 61 fields · synced Jul 24, 2026
  • FDA 510(k) K182420 1 fields · synced May 18, 2026