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Mozec™ NC

EUDAMEDFDA UDI

Class III (EU MDR)

Ref MNC22523

by Meril Life Sciences Pvt. Ltd.

Identity

Trade Name
Mozec™ NC EUDAMED
MozecTM NC Rx PTCA Balloon Dilatation Catheter FDA UDI
Generic Name
Coronary angioplasty balloon catheter, basic FDA UDI
Device Name
Mozec™ NC - Rx PTCA Balloon Dilatation Catheter EUDAMED
MozecTM NC Rx PTCA Balloon Dilatation Catheter, 2.25 mm x 23 mm, Rapid Exchange FDA UDI
Model / Reference
MNC22523 EUDAMEDFDA UDI
Description
MozecTM NC Rx PTCA Balloon Dilatation Catheter, 2.25 mm x 23 mm, Rapid Exchange FDA UDI

Identifiers

Catalog Number
MNC22523 FDA UDI
Primary DI / UDI-DI
18906029358162 EUDAMEDFDA UDI
Basic UDI-DI
B-18906029358162 EUDAMED
FDA Product Code
LOX FDA UDI
EMDN Code
C010401020101 PTCA BALLOON DILATION CATHETERS EUDAMED
GMDN Term
Coronary angioplasty balloon catheter, basic FDA UDI

Classification

Device Class
Class III EUDAMED
Class II FDA UDI
Regulation Number
870.5100 FDA UDI
Market of Registration
Türkiye EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 23 Millimeter FDA UDI
Outer Diameter — 2.25 Millimeter FDA UDI

Category: Coronary angioplasty balloon catheter, cutting/scoring

Mozec™ NC by Meril Life Sciences Pvt. Ltd. — Class III — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coronary angioplasty balloon catheter, cutting/scoring.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
IN-MF-000008308
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (2)

  • EUDAMED c636a124-a9c1-4ff0-a707-272eade680b2 61 fields · synced Jul 9, 2026
  • FDA UDI 56542ef7-d1e1-438a-a8a8-c311a594f052 37 fields · synced May 30, 2026