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Teknomek

EUDAMED

Class IIa (EU MDR)

Ref VCE220

by TEKNOMEK MEDİKAL MALZEMELERİ SAN. ve TİC. LTD. ŞTİ.

Identity

Trade Name
TEKNOMEK EUDAMED
Device Name
Silicone Injection and Extraction System (Silicone tube, Syringe, and 20G Ophthalmic Cannula) EUDAMED
Model / Reference
VCE220 EUDAMED

Identifiers

Primary DI / UDI-DI
08680548913882 EUDAMED
Basic UDI-DI
B-08680548913882 EUDAMED
EMDN Code
A060102 SURGICAL DRAINAGE CONNECTION MEDICAL TUBES EUDAMED

Classification

Device Class
Class IIa 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Suction/irrigation tubing, single-use

Teknomek by TEKNOMEK MEDİKAL MALZEMELERİ SAN. ve TİC. LTD. ŞTİ. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Suction/irrigation tubing, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
TR-MF-000018462

Sources (1)

  • EUDAMED cdacb360-d0b2-4582-ae23-535a8628696a 61 fields · synced Jun 18, 2026