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SUJ10 20GA Backflush/Extrusion Handpc softtip

EUDAMED

Class IIa (EU MDR)

Ref SUJ10

by Bausch & Lomb GmbH

Identity

Trade Name
SUJ10 20GA Backflush/Extrusion Handpc softtip EUDAMED
Device Name
Passive Aspiration/Backflush Extrusion Handpiece EUDAMED
Model / Reference
SUJ10 EUDAMED

Identifiers

Primary DI / UDI-DI
24058935005584 EUDAMED
Basic UDI-DI
4058935-130100-CB EUDAMED
EMDN Code
Q021101 OCCULAR IRRIGATION AND ASPIRATION CANNULAS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

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

SUJ10 20GA Backflush/Extrusion Handpc softtip by Bausch & Lomb GmbH — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Bausch & Lomb GmbH
EUDAMED SRN
DE-MF-000009142

Sources (1)

  • EUDAMED a035776a-18d9-42ab-9267-7535f0e793f9 61 fields · synced Aug 3, 2026