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Anodyne Surgical

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 9020-20BModel Chamber Maintainers

by Psi/Eye-Ko, Inc.

Identity

Trade Name
High Viscosity Fluid Cannula 20g, blunt EUDAMED
Anodyne Surgical FDA UDI
Generic Name
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use FDA UDI
Device Name
High Viscosity Fluid Cannula 20g, blunt FDA UDI
Model / Reference
9020-20B EUDAMEDFDA UDI
Chamber Maintainers EUDAMED
Description
High Viscosity Fluid Cannula 20g, blunt FDA UDI

Identifiers

Primary DI / UDI-DI
00840516117997 EUDAMEDFDA UDI
Basic UDI-DI
0840516190005Y EUDAMED
FDA Product Code
HMX FDA UDI
EMDN Code
Q021101 OCCULAR IRRIGATION AND ASPIRATION CANNULAS, SINGLE-USE EUDAMED
GMDN Term
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use 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

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

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

Anodyne Surgical by Psi/Eye-Ko, Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — 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 Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Psi/Eye-Ko, Inc.

Sources (2)

  • FDA UDI 42a4e590-b081-4510-964c-39c773b9ed55 34 fields · synced Jul 22, 2026
  • EUDAMED 7d800f49-34c0-4d72-b145-414d2cbdcab3 61 fields · synced Jul 22, 2026