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Marqueur scleral

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 17539X20Model 17249X1

by Moria S.A.

Identity

Trade Name
Marqueur scleral EUDAMED
ONE FDA UDI
Generic Name
Scleral marker, single-use FDA UDI
Device Name
Toric IOL pre-op marker, bubble level EUDAMED
Model / Reference
17249X1 EUDAMED
17539X20 EUDAMED
ONE S-Scleral marker X20 FDA UDI

Identifiers

Catalog Number
17539X20 FDA UDI
Primary DI / UDI-DI
03700483621897 EUDAMEDFDA UDI
Basic UDI-DI
37004836Markers3BX EUDAMED
FDA Product Code
HMR FDA UDI
EMDN Code
Q0299 OPHTHALMIC DEVICES - OTHER EUDAMED
GMDN Term
Scleral marker, single-use FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
886.4570 FDA UDI
Market of Registration
France 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Marqueur scleral by Moria S.A. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Moria S.A.
EUDAMED SRN
FR-MF-000000336

Sources (2)

  • EUDAMED fce2eead-1bd1-4747-8889-f6032fa93cc8 61 fields · synced Jun 18, 2026
  • FDA UDI b9b32f1a-4dbf-4089-9e24-35d05f405f91 33 fields · synced May 30, 2026