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C010401020101

EUDAMED

Class III (EU MDR)

Ref LNC20038Ref LNC22538

by Meril Life Sciences Pvt. Ltd.

Identity

Trade Name
C010401020101 EUDAMED
Device Name
Lineage™ NC - Rx PTCA Balloon Dilatation Catheter EUDAMED
Model / Reference
LNC20038 EUDAMED
LNC22538 EUDAMED

Identifiers

Primary DI / UDI-DI
18904224921891 EUDAMED
18904224922010 EUDAMED
Basic UDI-DI
B-18904224921891 EUDAMED
B-18904224922010 EUDAMED
EMDN Code
C010401020101 PTCA BALLOON DILATION CATHETERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Spain 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

C010401020101 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 (2)

  • EUDAMED 57443610-2efb-4717-9638-aafd1b13056b 61 fields · synced Jul 16, 2026
  • EUDAMED 5c3fa8e4-bd32-4925-9283-1fe35ba1b11d 61 fields · synced May 18, 2026