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Paximus™

EUDAMED

Class III (EU MDR)

Ref PO35P090050BModel UL 1350mm

by Meril Life Sciences Pvt. Ltd.

Identity

Trade Name
Paximus™ EUDAMED
Device Name
Paximus™ Balloon Catheter (OTW 0.035) EUDAMED
Model / Reference
UL 1350mm EUDAMED
PO35P090050B EUDAMED

Identifiers

Primary DI / UDI-DI
18904224925073 EUDAMED
Basic UDI-DI
B-18904224925073 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

Yes

EUDAMED

Category: Coronary angioplasty balloon catheter, cutting/scoring

Paximus™ 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 3dcbba32-89c4-4d94-a77c-021324cd8eaf 61 fields · synced Jun 18, 2026