← Back to catalogue

Eye Safety Two-Position, (577 nm)

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 65472

by Iridex Corporation

Identity

Trade Name
Eye Safety Two-Position, (577 nm) EUDAMED
Eye Safety Filter, Two-Position (577 nm) FDA UDI
Generic Name
General/multiple surgical diode laser system FDA UDI
Device Name
Eye Safety Filter (ESF) EUDAMED
For use on the Leica or Wild Dovetails OD3 @ 577 nm FDA UDI
Model / Reference
65472 EUDAMEDFDA UDI
Description
For use on the Leica or Wild Dovetails OD3 @ 577 nm FDA UDI

Identifiers

Primary DI / UDI-DI
00813125014490 EUDAMEDFDA UDI
Basic UDI-DI
081312501ESF8P EUDAMED
FDA Product Code
HQF FDA UDI
EMDN Code
Z12120280 THERAPEUTIC AND SURGICAL OPHTHOLMOLOGICAL TREATMENTS INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
General/multiple surgical diode laser system FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
886.4390 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Eye Safety Two-Position, (577 nm) by Iridex Corporation — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Iridex Corporation
EUDAMED SRN
US-MF-000029814
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED bc8300d1-472c-43ea-bc7c-b1eab34109cc 61 fields · synced Jun 18, 2026
  • FDA UDI e89d901f-aa00-472a-be45-0fac3f1e54cb 34 fields · synced May 30, 2026