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Sautter Air Injection Cannula

EUDAMED

Class IIa (EU MDR)

Ref 85050-6Ref 85050Y1-6

by Bausch & Lomb GmbH

Identity

Trade Name
Sautter Air Injection Cannula EUDAMED
Device Name
Cannula irrigation and or aspiration incl. Accessories EUDAMED
Model / Reference
85050-6 EUDAMED
85050Y1-6 EUDAMED

Identifiers

Primary DI / UDI-DI
04058935009038 EUDAMED
04058935009045 EUDAMED
Basic UDI-DI
B-04058935009038 EUDAMED
B-04058935009045 EUDAMED
EMDN Code
L1713 OCULAR IRRIGATION OR SUCTION CANNULAS, REUSABLE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Sautter Air Injection Cannula by Bausch & Lomb GmbH — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

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

Sources (2)

  • EUDAMED c7315518-1f91-43eb-ab90-266c95be35c1 61 fields · synced Jul 10, 2026
  • EUDAMED e34928fc-a6c8-4d15-9b07-4e6978282bf8 61 fields · synced May 19, 2026