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Rejenart

EUDAMED

Class III (EU MDR)

Ref RA-2-40Model REJENART - Sterile Sodium Hyaluronate Gel 2mL Prefilled Syringe (2,0%)

by İstem Medikal Tıbbi Cihaz ve Sanayi Ticaret Anonim Şirketi

Identity

Trade Name
REJENART EUDAMED
Device Name
REJENART - Sterile Sodium Hyaluronate Gel 2mL Prefilled Syringe (2,0%) EUDAMED
Model / Reference
REJENART - Sterile Sodium Hyaluronate Gel 2mL Prefilled Syringe (2,0%) EUDAMED
RA-2-40 EUDAMED

Identifiers

Primary DI / UDI-DI
08699415734031 EUDAMED
Basic UDI-DI
B-08699415734031 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

No

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

No

EUDAMED

Rejenart 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 4671b0fe-d9a4-4211-bba9-7fd55ec5ab21 61 fields · synced Oct 6, 2026