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Optiflush

EUDAMED

Class III (EU MDR)

Ref 1134Model Sterile 0,9% Sodium Chloride Solution, 20mL

by İstem Medikal Tıbbi Cihaz ve Sanayi Ticaret Anonim Şirketi

Identity

Trade Name
OPTIFLUSH EUDAMED
Device Name
Sterile 0,9% Sodium Chloride Solution, 20mL EUDAMED
Model / Reference
Sterile 0,9% Sodium Chloride Solution, 20mL EUDAMED
1134 EUDAMED

Identifiers

Primary DI / UDI-DI
05060222471441 EUDAMED
Basic UDI-DI
B-05060222471441 EUDAMED
EMDN Code
A02010299 INFUSION AND IRRIGATION SYRINGES - OTHER EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

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

Yes

EUDAMED

Optiflush by İstem Medikal Tıbbi Cihaz ve Sanayi Ticaret Anonim Şirketi — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
TR-MF-000017811

Sources (1)

  • EUDAMED fe6f1cfe-ec7a-4e3a-ac02-554cac75a1b6 61 fields · synced Oct 6, 2026