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Lacrimal Cannula 25g, curved

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 8000Model Lacrimal cannulas

by PSI/EYE-KO, Inc.

Identity

Trade Name
Lacrimal Cannula 25g, curved EUDAMED
Anodyne Surgical FDA UDI
Generic Name
Lacrimal procedural cannula FDA UDI
Device Name
Lacrimal Cannula 25g, curved FDA UDI
Model / Reference
Lacrimal cannulas EUDAMED
8000 EUDAMEDFDA UDI
Description
Lacrimal Cannula 25g, curved FDA UDI

Identifiers

Primary DI / UDI-DI
00840516106038 EUDAMED
00840516117393 EUDAMEDFDA UDI
Basic UDI-DI
0840516180005R EUDAMED
FDA Product Code
HMX FDA UDI
EMDN Code
Q021101 OCCULAR IRRIGATION AND ASPIRATION CANNULAS, SINGLE-USE EUDAMED
GMDN Term
Lacrimal procedural cannula FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
886.4350 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDEUDAMEDFDA 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use

Lacrimal Cannula 25g, curved by Psi/Eye-Ko, Inc. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PSI/EYE-KO, Inc.
EUDAMED SRN
US-MF-000022109
Authorised Representative
Advena Limited MT-AR-000000234

Sources (3)

  • EUDAMED 1f787d3a-f414-4064-929d-b8b90273f5d6 61 fields · synced Jul 18, 2026
  • FDA UDI 74f1d94d-2979-4661-8959-ce875e242d3b 34 fields · synced May 30, 2026
  • EUDAMED c95333e4-3671-4ca1-9b98-02c566f5c89e 61 fields · synced Jul 18, 2026