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Xpedient™

EUDAMED

Class III (EU MDR)

Ref XPD35025

by Meril Life Sciences Pvt. Ltd.

Identity

Trade Name
Xpedient™ EUDAMED
Device Name
Xpedient™ - Rx PTCA Balloon Dilatation Catheter EUDAMED
Model / Reference
XPD35025 EUDAMED

Identifiers

Primary DI / UDI-DI
18906029356861 EUDAMED
Basic UDI-DI
B-18906029356861 EUDAMED
EMDN Code
C010401020101 PTCA BALLOON DILATION CATHETERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany 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

Xpedient™ by Meril Life Sciences Pvt. 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
IN-MF-000008308
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 4cce1579-d974-4dc2-bb31-7935c5ae54b2 61 fields · synced Jun 20, 2026