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Mesire™ Illuminus

EUDAMEDFDA UDI

Class I (EU MDR)

Ref MSI083

by Meril Life Sciences Pvt. Ltd.

Identity

Trade Name
Mesire™ Illuminus EUDAMED
MesireTM Illuminus - Sinus Light Wire FDA UDI
Generic Name
Paranasal sinus-illumination light guide cable FDA UDI
Device Name
Mesire™ Illuminus Sinus Light wire EUDAMED
MesireTM Illuminus -Sinus Light Wire, 0.83 mm FDA UDI
Model / Reference
MSI083 EUDAMEDFDA UDI
Description
MesireTM Illuminus -Sinus Light Wire, 0.83 mm FDA UDI

Identifiers

Catalog Number
MSI083 FDA UDI
Primary DI / UDI-DI
18904224901541 EUDAMEDFDA UDI
Basic UDI-DI
B-18904224901541 EUDAMED
510(k) Number
K172737 FDA UDI
FDA Product Code
LRC FDA UDI
EMDN Code
Q030199 NASOPHARYNGEAL DEVICES - OTHER EUDAMED
GMDN Term
Paranasal sinus-illumination light guide cable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
874.4420 FDA UDI
Market of Registration
Germany 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
Outer Diameter — 0.83 Millimeter FDA UDI

Mesire™ Illuminus by Meril Life Sciences Pvt. Ltd. — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

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 073cfb2c-31f1-4306-b01e-0d96177c62d9 61 fields · synced Jul 31, 2026
  • FDA UDI e8d5a2f2-23cb-496c-a6de-d8d4926a291a 38 fields · synced May 27, 2026