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Mesire™ Latch

EUDAMEDFDA UDI

Class I (EU MDR)

Ref MSL

by Meril Life Sciences Pvt. Ltd.

Identity

Trade Name
Mesire™ Latch EUDAMED
MesireTM Latch - Catheter Holding System FDA UDI
Generic Name
Paranasal sinus guide-catheter handle FDA UDI
Device Name
Mesire™ Latch Catheter Holding System EUDAMED
MesireTM Latch - Catheter Holding System FDA UDI
Model / Reference
MSL EUDAMEDFDA UDI
Description
MesireTM Latch - Catheter Holding System FDA UDI

Identifiers

Catalog Number
MSL FDA UDI
Primary DI / UDI-DI
18904224905709 EUDAMEDFDA UDI
Basic UDI-DI
B-18904224905709 EUDAMED
89042249CHSZT EUDAMED
Direct Marketing DI
18904224905709 EUDAMED
510(k) Number
K172737 FDA UDI
FDA Product Code
LRC FDA UDI
EMDN Code
Q030199 NASOPHARYNGEAL DEVICES - OTHER EUDAMED
GMDN Term
Paranasal sinus guide-catheter handle 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

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

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

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

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 (3)

  • EUDAMED e26a28da-e699-4129-a3a8-67b9b1492f8d 61 fields · synced Jul 14, 2026
  • FDA UDI eef49c58-7590-460d-a7d4-cb3ad86dd300 37 fields · synced May 30, 2026
  • EUDAMED befd72c3-4896-4667-9ecc-5c3a2aef1dd8 61 fields · synced Jul 14, 2026